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United States · US · US:82038-006_1b3332f9-96b6-b71b-e063-6394a90a27be

Protectif Fair Tint

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerDerma Research Group Inc.
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    8203800602
    1 BOTTLE, PUMP in 1 CARTON (82038-006-02) / 100 g in 1 BOTTLE, PUMP (82038-006-01)
  • ndc11
    8203800604
    1 BOTTLE, PUMP in 1 CARTON (82038-006-04) / 30 g in 1 BOTTLE, PUMP (82038-006-03)

Annotations

UNII (FDA Substance ID)
15FIX9V2JP
TITANIUM DIOXIDE
RxCUI 38323
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "15FIX9V2JP",
    "rxcui": "38323",
    "inchikey": "SOQBVABWOPYFQZ-UHFFFAOYSA-N",
    "display_name": "TITANIUM DIOXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "1a8c8804-1d6b-b5a5-e063-6394a90a1260": {
      "match": "brand_token",
      "title": "PROTECTIF FAIR TINT (ZINC OXIDE AND TITANIUM DIOXIDE) CREAM [DERMA RESEARCH GROUP INC.]",
      "spl_version": "2",
      "published_date": "2024-06-20"
    }
  },
  "productid": "82038-006_1b3332f9-96b6-b71b-e063-6394a90a27be",
  "productndc": "82038-006",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Protectif Fair Tint",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Zinc Oxide and Titanium Dioxide",
  "start_marketing_date": "20240510",
  "active_numerator_strength": "6.5; 8.6"
}

Access this data programmatically

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