HS 33.03 – 33.07

Cosmetics & personal care

Cosmetics sell like fast-moving consumer goods and clear customs like regulated ones. The bulk is rarely what holds a shipment up — the safety file, the label and the notification are, and every destination wants them assembled a different way.

Unlabelled serum dropper, cream jar and perfume flacon
§ What we trade

What we trade in this category

  • Face care emulsions and serums an emulsion is a stability problem in a jar, and every pack change reopens stability, compatibility and the preservative challenge test
  • Alcoholic fragrance, EDT and EDP UN 1266, Class 3 flammable liquid, so the packing and the lane are decided before the juice is
  • Hair care in litre formats low value per kilo, which means it only works as full containers on a sea lane and dies on air freight
  • Sun care SPF and UVA figures have to be earned in a laboratory, and the permitted filter list changes at every border
  • Bath, body and deodorants (HS 3307) the bulk is cheap; the pump, the valve and the carton set both the price and the lead time
  • Colour cosmetics shade drift between production runs, plus pigment and talc purity files the buyer will ask to see
  • Gift sets and travel formats a separate bill of materials, a set classification question at import, and an August build for a December sell
§ How we select

How a supplier and a product get chosen.

01

Screen the formula first

Take the ingredient list to the destination's annexes before you take a sample: Annexes II to VI for the EU, the IECIC inventory for mainland China, the ASEAN annexes for Singapore. A preservative or a UV filter that fails at this stage costs one email. The same failure found after the safety report is written costs the file, the artwork and the batch.

02

Audit the plant, not the sample

Any factory can make a good sample. Ask for ISO 22716 evidence, then look at the water system, the microbiological laboratory, the batch records, the retained samples and whether challenge testing is run in-house or bought in. The document that matters most is the change-control procedure, because it is the only thing standing between a buyer and a silent preservative substitution.

03

Separate bulk from pack

Bulk and primary pack are usually two suppliers with different minimums and different lead times. Establish who owns the mould and what the cavitation is, whether the quoted price includes the pump and the decoration, and what the component lead time does over Chinese New Year. Then run stability and compatibility on the actual pack, not on a laboratory jar.

04

Cost the file, not the unit

Per market: safety assessment, stability, compatibility, challenge test to ISO 11930, the microbiological panel, SPF work where it applies, artwork and translation, notification fees, the responsible person, packaging producer-responsibility registration. On a first order the file frequently costs more than the goods, which is why SKU count moves landed cost more than volume does.

05

Trial order, then contract

Buy a trial batch, keep retained samples, and agree the specification and the format of the certificate of analysis before anything scales. Only then sign supply terms that fix the formula and the components by supplier and grade, require written notice of any change, and state the minimum remaining shelf life on delivery.

§ Development

Development and design.

Design

Formulation brief written as a specification

We write the brief as targets rather than adjectives: texture, pH range, viscosity at a stated temperature, fragrance dosage, colour standard, and only the claims that can be substantiated in the destination market. The bill of materials is version-controlled by INCI name, percentage, supplier and grade, because that is the level at which compliance is actually decided.

Design

Pack, tooling and decoration

Glass, PET or airless; pump dosage and the number of primes before first dose; tooling ownership, cavitation and who pays for it; silk-screen, hot foil, sleeve or label, and how the adhesive behaves on an oily surface. Each of these changes the stability and compatibility work, so we settle the pack before we lock the formula rather than after.

Design

Artwork and localisation

One master die-line, then a layer per market: INCI in descending order, nominal content, the period-after-opening symbol or the date of minimum durability, batch code, warnings, product function where the presentation is not obvious, and the responsible person or importer. Serbian, Arabic and Chinese versions are approved artworks in their own right, and where a market allows an over-sticker it is drawn with the pack, not improvised at the port.

Design

Fragrance and colour control

For anything scented we hold the IFRA conformity certificate and the allergen declaration from the fragrance house, and we take fresh ones when the house reformulates, because a supplier-side reformulation quietly invalidates the label. Shade work runs against a physical standard with an agreed tolerance, since the second production run is where colour drifts.

§ Our part

What we do that a broker does not.

A

We build and hold the safety file

We commission the safety assessor, assemble the product information file against the actual bill of materials rather than the marketing copy, and make the filing the destination requires: CPNP for the EU, the responsible-person and notification obligations under the Serbian rulebook, HSA notification through the Singapore notifier, NMPA filing or registration through the domestic responsible person, SFDA through a licensed Saudi establishment and then emirate-level registration in the UAE. Where an EU establishment is needed to carry the responsible-person role, the group has one in Portugal.

B

Change control on the factory

We hold the approved bill of materials, the component specifications and the artwork masters, and the supply agreement requires written notice before any of them move. Retained samples come out of every batch, and the certificate of analysis is read line by line against the specification before the balance payment is released.

C

Pre-shipment inspection as a release gate

We book the inspection and inspect what actually fails in this category: fill weight, cap torque and leak, pump function after transport simulation, label placement and legibility, batch code and period-after-opening printed and correct, carton drop, and remaining shelf life against what the contract says. We hold the balance payment until it passes.

D

Dangerous goods and heat

Alcoholic fragrance, aerosols and nail products move as dangerous goods, and an alcohol gel sold on a germ-kill claim leaves the cosmetics regime for the biocides one. We produce the safety data sheet, decide limited quantity against fully regulated, arrange UN-specification packing where that choice requires it, the marks and the transport document, and pick the lane against the surcharge instead of assuming air freight is available. Emulsions and anything wax-based get a routing and a stow chosen for temperature.

E

We sell into the same shelves we ship to

We own consumer brands and put them on shelves ourselves, so registrations, packaging producer-responsibility registration, marketplace listing content, retailer artwork packs and consumer complaint handling are work we already do for our own goods. A buyer gets the trade file and the retail file from the same people, which is not the same thing as a broker forwarding a factory's PDF.

§ Documents

What the paperwork actually is.

The document set below is what this category needs to clear. We raise it rather than forwarding a checklist.

  • EU — Regulation (EC) No 1223/2009. A responsible person established in the EU and named on the pack, a product information file kept available for ten years, a cosmetic product safety report signed by a qualified safety assessor, CPNP notification before the first unit is sold, and Article 19 labelling: INCI list in descending order, nominal content, period-after-opening symbol or date of minimum durability, batch number, function, warnings and, on imported product, the country of origin.
  • EU — the annexes move constantly and reformulation deadlines are the real cost. Recent examples: the vitamin A, arbutin and kojic acid restrictions under Regulation (EU) 2024/996; the TPO prohibition under Regulation (EU) 2025/877, which came with no sell-through period; the expanded fragrance-allergen declarations under Regulation (EU) 2023/1545, biting on products placed on the market from 31 July 2026 with existing stock saleable until 31 July 2028; the synthetic polymer microparticle restriction under Regulation (EU) 2023/2055. Claims sit under Regulation (EU) 655/2013, aerosol dispensers under Directive 75/324/EEC, and packaging carries producer-responsibility registration in every member state you sell into.
  • Serbia — the Law on Items of General Use and the Rulebook on Cosmetic Products (Sl. glasnik RS 60/2019 and its amendments) are a close copy of the EU regime, but they are national. The importer is the responsible person and must be seated in Serbia, must hold the product information file and safety report, must clear each consignment through the border sanitary inspection before customs will release it, and must carry the responsible person, the warnings and the product function in Serbian. The Ministry of Health's sanitary inspection enforces at the border and in store, and an EU-compliant label is not automatically a Serbian one.
  • Hong Kong and Singapore — Hong Kong has no pre-market registration for ordinary cosmetics; the exposure is in the claim, since anything presented as treating a condition falls under the Pharmacy and Poisons Ordinance and the Undesirable Medical Advertisements Ordinance, with general safety under the Consumer Goods Safety Ordinance. Singapore runs the ASEAN Cosmetic Directive: notification to the Health Sciences Authority by a locally incorporated company before sale, renewed annually, with the product information file held and producible on demand.
  • Mainland China — the Cosmetic Supervision and Administration Regulation. General cosmetics are filed; special cosmetics (sunscreen, hair dye, perming, freckle-removing and whitening, anti-hair-loss and new efficacy claims) are registered, which is a longer and more expensive route. You need a domestic responsible person, every ingredient on the IECIC inventory, a full safety assessment report since the simplified version was withdrawn on 1 May 2025, and efficacy substantiation with a summary published on the platform. The animal-testing exemption for imported general cosmetics needs a GMP certificate from the authority of the producing country and a safety assessment that carries the product on its own, and it is closed to children's products and to anything holding a new ingredient still under monitoring. Cross-border e-commerce into a bonded warehouse is a separate route with separate paperwork and separate economics.
  • Gulf and per-shipment documents — the GCC technical regulation is modelled on the EU one; the UAE requires an ECAS certificate of conformity and then emirate-level product registration, Saudi Arabia requires SFDA notification, Arabic labelling is mandatory and halal certification is often demanded from a body the destination authority recognises. Every shipment then carries the ordinary file: commercial invoice and packing list, certificate of origin or a preferential proof where one applies, batch certificates of analysis, a free sale certificate where the destination asks for one, and the safety data sheet and dangerous goods declaration for anything flammable.
§ Corridors

How it moves.

European skincare and fragrance move east — from Porto and Belgrade into Hong Kong, Singapore and Greater China, where an EU origin and a legible ingredient list carry commercial weight, and where duty is only part of the landed cost: Hong Kong is a free port, while the mainland adds VAT and a 15% consumption tax on cosmetics above a per-millilitre and per-piece price threshold that is not recoverable against input VAT. The return lane is Asian contract manufacture, bulk and components into the EU, Serbia and the Gulf, and Serbia is the useful middle of it — goods manufactured there, worked beyond simple packing, reach the EU under the Stabilisation and Association Agreement, CEFTA neighbours and the Eurasian Economic Union under Serbia's own free trade agreement, where the duty preference is the easy half and conformity to the Customs Union technical regulation on perfumery and cosmetic products is the rest, provided the rules of origin are genuinely met and documented.

See the lanes we run

§ Questions

What buyers ask first.

Can you act as our responsible person in the EU?

The role has to sit with a legal person established in the EU and be printed on the pack, so it cannot be handled from Hong Kong. The group has an EU establishment through its Portuguese entity, so we can carry it, or we can build the product information file to the standard your own responsible person will accept and hand it over. Either way the file has to match what the factory is actually making, which is why we insist on holding change control alongside it.

The factory says the formula is EU compliant. Is that enough?

No. Compliance is a file, not an adjective, and the statement is worth exactly as much as the assessor's report behind it. Ask for the cosmetic product safety report, the assessor's qualifications and the full bill of materials by INCI name and percentage, then check it against the current annexes yourself, because the annexes have moved more than once in the past two years. A factory statement about the EU also says nothing about the IECIC inventory or the ASEAN annexes.

What remaining shelf life will we actually receive?

Whatever you wrote into the contract, so write it in. Products with a durability over thirty months carry a period-after-opening symbol rather than a date, unless opening is not a concept - single-use, sealed and pressurised packs, which is not the same as unlimited shelf life, and retailers still enforce their own minimum at goods-in. Work backwards from the real calendar: production, quality release, a notification queue in the destination, then the sailing your carrier is quoting this month, not the one on last year's schedule.

Why can't we simply air-freight the fragrance?

Alcoholic fragrance is UN 1266, Class 3, so it moves under the air dangerous goods rules with quantity limits per package, a surcharge, and forwarders and airlines that will decline it outright in peak season. Sea in properly packed limited-quantity or fully regulated form is usually the answer, and it has to be planned around the gift-set calendar rather than discovered in October. Aerosols and nail products carry their own class and their own restrictions.

§ Other sectors

Moving cosmetics & personal care?

Tell us the product, the origin and the destination. We come back with the classification, the document set and a realistic timeline.

Open a file with us
§ Two minutes

Not ready to write a brief?

Leave three lines and we will come back with the corridor, the customs position and a realistic timeline for whatever you are moving.

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