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Shamp👀 · Deep Dive · Product Safety · 公開 2026-05-01 Updated 2026-05-01

Global Cosmetic Ingredient Regulations: Eu Annex Ii Iii — Deep Dive

要約

In-depth analysis of eu annex ii iii within global cosmetic ingredient regulations for salons.

📑 目次
  1. 1. Context
  2. 2. Common pitfalls
  3. 3. Authority-recommended solutions
  4. 4. Operator dialogue
    1. 🦉 & 🐥 & 🐮 — Salon operator dialogue
  5. 5. KPI targets
  6. Primary sources (national & international authorities)
    1. Related Articles
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1. Context

The global cosmetic ingredient regulatory landscape is a patchwork of overlapping but non-identical systems[1]. The EU bans 1,730 substances (Annex II) and restricts 370 more (Annex III); the US FDA historically permitted most ingredients unless proven harmful, though MoCRA 2022 begins to change this; Japan maintains its own positive/negative lists under the Pharmaceutical and Medical Device Act[2].

This deep dive focuses on eu annex ii iii — one of the most critical sub-areas within global cosmetic ingredient regulations.

2. Common pitfalls

  1. EU Annex II/III not consulted when purchasing new products
  2. US FDA MoCRA 2022 requirements unknown to US salons
  3. Japan PMDA positive/negative list not checked
  4. Product imported from non-EU country assumed to meet EU standards
  1. General solution
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4. Operator dialogue

🦉 & 🐥 & 🐮 — Salon operator dialogue

🐥
Piyo: Poppo, what's the difference between EU Annex II and Annex III?
🦉
Poppo: Annex II is the prohibited list — over 1,600 substances that must never appear in a cosmetic product sold in the EU. Annex III is the restricted list — substances allowed only up to specified concentrations (like PPD at max 2% in hair dyes). If a product violates either, it's illegal to use, full stop.
🐥
Piyo: What about products from the US or Asia?
🦉
Poppo: FDA regulates differently — until MoCRA (2022), there was no mandatory registration. Japan's Pharmaceutical Affairs Act has its own positive list. A salon using international products must verify compliance with their own jurisdiction's regulations.
🐮
Mou: Strong, kind, beautiful — knowing the rules behind your products is what separates a professional from an amateur.

5. KPI targets

IndicatorBaselineTargetTimeMeasurement
Annex II compliance (prohibited list)Variable100% products checked1 monthProduct audit
Annex III concentration verificationVariable100% restricted substances1 monthLab/SDS cross-check
FDA MoCRA registration statusUnknown100% US-sourced verified3 monthsRegistration check
INCI label accuracyVariable100%1 monthLabel audit
New regulation awareness lagVariable<30 days from publicationOngoingRegulatory alert feed

Primary sources (national & international authorities)

  1. WHO Guidelines on Hand Hygiene in Health Care (2009). https://www.who.int/publications/i/item/9789241597906
  2. EU Regulation (EC) No 1223/2009 on cosmetic products. https://eur-lex.europa.eu/eli/reg/2009/1223/oj
  3. FDA Modernization of Cosmetics Regulation Act (MoCRA, 2022). https://www.fda.gov/cosmetics/cosmetics-laws-regulations/modernization-cosmetics-regulation-act-2022-mocra
  4. Cosmetic Ingredient Review (CIR) — 4,740+ ingredient assessments. https://www.cir-safety.org/ingredients

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製品成分をEU Annex II/III、FDA、CIRデータベースと照合 — 無料PDFレポートを即時生成。

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重要な免責事項： MmowWは美容衛生認証機関ではありません。上記の内容は、各国当局の一次ソース（WHO・FDA・EU規則1223/2009・各国衛生当局）から抽出した教育目的のベストプラクティス情報です。最終責任はサロン事業者および所轄当局にあります。常に一次ソースおよびお住まいの規制当局でご確認ください。
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澤井 隆行 — 行政書士

行政書士・MmowW創業者。世界中のサロン衛生コンプライアンスを極楽にする。

安全で、愛される。