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United States · US · US:72043-2920_79386a40-776e-47d1-8909-88776673d1a9
UV Daily Deep Tint
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCP Skin Health Group, Inc.
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11720432920150 g in 1 BOTTLE (72043-2920-1)
- ndc1172043292022 g in 1 PACKET (72043-2920-2)
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": {
"02e71602-13e1-43b3-9cba-a75e46cccacc": {
"match": "brand_token",
"title": "UV DAILY HYDRATION TINTED (OCTISALAT AND ZINC OXIDE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC]",
"spl_version": "1",
"published_date": "2026-05-20"
}
},
"productid": "72043-2920_79386a40-776e-47d1-8909-88776673d1a9",
"productndc": "72043-2920",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; ZINC OXIDE",
"proprietary_name": "UV Daily Deep Tint",
"active_ingred_unit": "g/1000g; g/1000g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "octinoxate, zinc oxide sunscreen",
"start_marketing_date": "20240509",
"active_numerator_strength": "750; 900"
}Related drugs
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