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United States · US · US:62082-057_0973bc65-d2e0-0fef-e063-6294a90a1290
PHARMACA Natural Mineral Sunscreen SPF-50
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharmaca Integrative Pharmacy, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc116208205703100 mL in 1 TUBE (62082-057-03)
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": {
"51e6cd7a-5c9a-4666-9021-ade42eb064cd": {
"match": "brand_token",
"title": "PHARMACA NATURAL MINERAL SUNSCREEN SPF-50 (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [PHARMACA INTEGRATIVE PHARMACY, INC.]",
"spl_version": "2",
"published_date": "2023-11-06"
}
},
"productid": "62082-057_0973bc65-d2e0-0fef-e063-6294a90a1290",
"productndc": "62082-057",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TITANIUM DIOXIDE; ZINC OXIDE",
"proprietary_name": "PHARMACA Natural Mineral Sunscreen SPF-50",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "TITANIUM DIOXIDE, ZINC OXIDE",
"start_marketing_date": "20190520",
"active_numerator_strength": "60; 225"
}Access this data programmatically
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