What should a real COA include for body lotion, body wash, and body scrub?

A real COA for body lotion, body wash, and body scrub in SEA should include product identification, batch number, manufacturing date, expiration date, test results for microbial limits, heavy metals, pH, active ingredients, and compliance statements. It must be issued by the manufacturer with clear specifications.

SEA buyer view Launch planning Updated: June 2, 2026
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Best for
US brand owners, Amazon/FBA sellers, distributors, and private label buyers
Core intent
Who submits, what data is needed, and how to plan timelines before production

Quick Answer (for busy buyers)

Here’s the buyer-first summary. If your brand name is on the label, you usually act as the responsible person and must ensure the listing is submitted and kept current.

  • A COA for body care products in SEA must start with basic product info: name, batch number, manufacturing and expiry dates for traceability.
  • Key test results include microbial limits (e.g., total aerobic count under 1000 CFU/g), heavy metals (lead, arsenic, mercury within ASEAN limits), pH (4.0-7.0 for lotion, 5.5-6.5 for wash), and active ingredient concentrations.
  • For body scrub, particle size distribution and abrasiveness tests are added.
  • Compliance requires alignment with ASEAN Cosmetic Directive or local norms like BPOM in Indonesia or FDA in Thailand.
  • We support by conducting in-house or accredited lab testing, with sampling timelines of 2-4 weeks and production lead times of 6-8 weeks post-approval.
  • MOQ affects testing; batches under 10,000 units may have streamlined checks, while larger runs require full analysis.
  • Packaging compatibility tests, such as leakage risk from pump seals or label adhesion in humid SEA climates, are also documented.
  • Our QA ensures COAs are auditable, but final regulatory approval depends on authorities, so we recommend early documentation review.
Buyer outcome
A launch-ready compliance plan: inputs collected, roles assigned, and update cadence defined.
Most common blocker
Missing facility information + inconsistent ingredient/label snapshots across SKUs.
⚠️
This page is a practical buyer guide. For definitive requirements and updates, use FDA resources and qualified regulatory counsel.
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