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United States · US · US:72043-6808_b988dc70-eb19-4c6d-935e-74439188a438
EltaMD UV SPF35
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
- ndc1172043680822 g in 1 PACKET (72043-6808-2)
- ndc11720436808385 g in 1 TUBE (72043-6808-3)
- ndc117204368088226 g in 1 TUBE (72043-6808-8)
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": "72043-6808_b988dc70-eb19-4c6d-935e-74439188a438",
"productndc": "72043-6808",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; ZINC OXIDE",
"proprietary_name": "EltaMD UV SPF35",
"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": "75; 70"
}Related drugs
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