Protectif Deep Tint

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
8203800502
1 BOTTLE, PUMP in 1 CARTON (82038-005-02) / 100 g in 1 BOTTLE, PUMP (82038-005-01)
ndc11
8203800504
1 BOTTLE, PUMP in 1 CARTON (82038-005-04) / 30 g in 1 BOTTLE, PUMP (82038-005-03)

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": "82038-005_19b18cbb-b098-266a-e063-6294a90a81a8",
  "productndc": "82038-005",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
  "proprietary_name": "Protectif Deep 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": "20240509",
  "active_numerator_strength": "6.5; 8.6"
}

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