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Permitted list with conditionsBinding ruleUSOriginal is EnglishOfficial-source import checked

D&C Red No. 22

D&C Red No. 22. The color additive D&C Red No. 22 shall conform in identity and specifications to the requirements of § 74.1322 (a)(1) and (b) of this chapter. [47 FR 53847, Nov. 30, 1982]

All United States recordsCompare all marketsOpen official source

Regulatory decision and full conditions

Status
Permitted list with conditions
Legal role
Binding rule
Regulatory summary
D&C Red No. 22. The color additive D&C Red No. 22 shall conform in identity and specifications to the requirements of § 74.1322 (a)(1) and (b) of this chapter. [47 FR 53847, Nov. 30, 1982]
Conditions and restrictions
D&C Red No. 22. The color additive D&C Red No. 22 shall conform in identity and specifications to the requirements of § 74.1322 (a)(1) and (b) of this chapter. [47 FR 53847, Nov. 30, 1982]

Substance identity

Official source name
D&C Red No. 22
CAS
Not supplied in this source row
EC
Not supplied in this source row
Identity mapping
standalone:official_cfr_section
Search this identity across the site

Cross-market snapshot for this identity

Exact linked records currently present in this site. An absent market means no imported exact match, not permission to use the substance.

1 market dataset

United States

Current record
Permitted list with conditions

1 linked record · 1 with specific conditions

Open supporting record
No unique stored chemistry profile yet. The regulatory record above remains valid; formula, structure and physical-property fields are not guessed from a name-only match. Research this identity directly in PubChem.

Official source and provenance

Registered source
US FDA cosmetic ingredient framework
Source reference
21 CFR 82.1322
Source record ID
82.1322
Source version
2026-08-27
Source language
English
Translation status
Original is English
Source updated
2026-08-27
Snapshot checked
2026-08-30 04:30 UTC
Validation method
eCFR XML subpart/section parse; 99 records
SHA-256
25a55a997379f510077dfb234fe3f366e8a1429cec3d0b20fe4b60e2baf3c36d

Registered dataset notes

Dataset coverage
Federal ingredient framework, prohibited/restricted examples and color-additive rules
Authority note
The US has no EU-style general approved-ingredient catalogue; MoCRA listing is not approval
Inspect the exact official sourceRegulator guidance

How this record fits the market dataset

99
current United States records
90
records marked Permitted list with conditions
99
records from this source version
15
market records with CAS identity

Status distribution

Permitted list with conditions: 90Prohibited: 9

Condition text is present on 90 of 99 current records. An empty condition field is interpreted according to the record type above; it is never converted into an unrestricted-use claim.

United States market context

Complete enumerated federal ingredient rules

Coverage version: eCFR Title 21 issue date 27 August 2026

All cosmetic prohibitions/restrictions in Part 700 Subpart B and cosmetic-use colour additive listings in Parts 73, 74 and 82.

Verification checklist

  1. Search Part 700 and all relevant colour-additive parts.
  2. Confirm colour additive identity, permitted uses, limits and certification status.
  3. Assess safety and adulteration under the FD&C Act.
  4. Complete MoCRA facility/product, adverse-event and label obligations where applicable.

Official market sources

Verification workflow and record completeness

Before using this result in a compliance decision

  1. Confirm that “D&C Red No. 22” and every CAS/EC identifier refer to the material in your supplier specification.
  2. Search Part 700 and all relevant colour-additive parts.
  3. Confirm colour additive identity, permitted uses, limits and certification status.
  4. Assess safety and adulteration under the FD&C Act.
  5. Complete MoCRA facility/product, adverse-event and label obligations where applicable.
  6. Document the source version and recheck the regulator before manufacture, notification or market placement.

Fields available in this record

  • Official substance nameAvailable
  • CASNot supplied
  • ECNot supplied
  • Separate condition textAvailable
  • Effective dateNot supplied
  • Snapshot hash and methodAvailable

Questions this page answers

This identity appears on a market positive list for the list function represented by the source record. Confirm that the intended function and product use fall within the list scope and every stated condition.

Positive-list presence is purpose-specific and is not blanket approval for every cosmetic use. FDA has no general approved-cosmetic-ingredient catalogue; absence from these sections is not approval or proof of safety.

The record cites 21 CFR 82.1322, source version 2026-08-27. Open the official source.

No. CAS helps resolve identity, but jurisdictions can classify the same substance differently and can apply different product scopes, limits, warnings and transition dates.

Stable citation

D&C Red No. 22. 21 CFR 82.1322. United States. Source version 2026-08-27. CosIng Checker regulatory record: https://cosingchecker.com/regulations/us/records/800/

Cite the regulator as the legal authority. This page is a structured evidence index and verification aid, not a substitute for the official text or professional legal assessment.

Interpretation and limits for United States

This identity appears on a market positive list for the list function represented by the source record.

Confirm that the intended function and product use fall within the list scope and every stated condition.

How to interpret the legal role

The cited row forms part of a binding rule or legally incorporated list for this market.

Evidence on this page

  • Recorded outcome: Permitted list with conditions
  • Legal role: Binding rule
  • Source version: 2026-08-27

What it does not prove

FDA has no general approved-cosmetic-ingredient catalogue; absence from these sections is not approval or proof of safety.

Further authoritative substance research

These sources can add identity, safety, exposure or hazard context. A link is not evidence that the database contains this exact substance, and none of these sources overrides the market decision above.

Cosmetic Ingredient Review safety assessments

Expert Panel conclusions, assessed ingredient groups, use conditions, dates and report documents

Independent expert review considered by FDA; not a government approval or binding market rule

Research this identity at the source

FDA Global Substance Registration System

UNII identifiers, preferred names, substance types, codes and public substance relationships

Identity registry only; UNII availability does not imply FDA review or approval

Research this identity at the source

ILO/WHO International Chemical Safety Cards

Hazards, symptoms, first aid, storage, incompatibilities and physical properties for covered chemicals

International occupational chemical-safety reference; not cosmetic-use approval

Research this identity at the source

Japan NITE-CHRIP

Chemical identity, Japanese and foreign legal lists, GHS hazards and exposure-related information

Chemical-management evidence; cosmetic status remains governed by the applicable MHLW standard and market rules

Research this identity at the source

NIOSH Pocket Guide to Chemical Hazards

REL, PEL, IDLH, properties, exposure routes, symptoms, target organs, first aid and measurement methods for covered workplace chemicals

US occupational-health guidance and limits; not a cosmetic ingredient decision

Research this identity at the source

OECD eChemPortal

Gateway to authority-owned physical-property, fate, ecotoxicity, toxicity, exposure and GHS records

Discovery gateway; each linked authority remains responsible for its data

Research this identity at the source

US EPA CompTox CTX APIs

API key required for import

DTXSID identity, experimental and predicted properties, toxicity, bioactivity, exposure and environmental data

Scientific and computational evidence; predictions must remain labelled and do not determine cosmetic legality

Research this identity at the source