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United States · US · US:72043-6806_b25c8e67-afb2-4a2f-9335-e37ea4779887
EltaMD UV Daily Tinted
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 · 3
- ndc11720436806148 g in 1 BOTTLE (72043-6806-1)
- ndc1172043680622 g in 1 PACKET (72043-6806-2)
- ndc11720436806514 g in 1 BOTTLE (72043-6806-5)
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": {
"b9b5f3ef-bd38-4147-847a-af79da1d9cd6": {
"match": "brand_token",
"title": "ELTAMD UV DAILY TINTED SPF40 (ZINC OXIDE AND OCTINOXATE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.]",
"spl_version": "6",
"published_date": "2026-04-20"
}
},
"productid": "72043-6806_b25c8e67-afb2-4a2f-9335-e37ea4779887",
"productndc": "72043-6806",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; ZINC OXIDE",
"proprietary_name": "EltaMD UV Daily Tinted",
"active_ingred_unit": "g/1000g; g/1000g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "octinoxate, zinc oxide sunscreen",
"start_marketing_date": "20240531",
"active_numerator_strength": "750; 900"
}Related drugs
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