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United States · US · US:63750-015_26322aba-bc7d-2fa5-e063-6394a90a1e72
Vivant Day Treatment SPF 15
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerVivant Pharmaceuticals, LLC
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11637500150389 mL in 1 BOTTLE (63750-015-03)
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"10b923cc-1486-cd97-e063-6294a90a95d1": {
"match": "brand_token",
"title": "VIVANT TRUE TONE FORTE (HYDROQUINONE) GEL [VIVANT PHARMACEUTICALS, LLC]",
"spl_version": "3",
"published_date": "2025-07-28"
}
},
"productid": "63750-015_26322aba-bc7d-2fa5-e063-6394a90a1e72",
"productndc": "63750-015",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE",
"proprietary_name": "Vivant Day Treatment SPF 15",
"active_ingred_unit": "g/100mL; g/100mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octinoxate 7.50% Octisalate 5.00%",
"start_marketing_date": "20240201",
"active_numerator_strength": "7.5; 5"
}Related drugs
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Access this data programmatically
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