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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
- ndc1182038006021 BOTTLE, PUMP in 1 CARTON (82038-006-02) / 100 g in 1 BOTTLE, PUMP (82038-006-01)
- ndc1182038006041 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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