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United States · US · US:52993-001_4354515e-3730-41be-e063-6294a90afc67
Zinka Clear Zinc Oxide Sunscreen
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZinka, Inc.
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11529930010385.1 g in 1 TUBE (52993-001-03)
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": {
"7b097f5e-8127-49e6-8a77-4ee1fded5ff1": {
"match": "brand_token",
"title": "ZINKA CLEAR ZINC OXIDE SUNSCREEN (OCTINOXATE, ZINC OXIDE, OCTISALATE, OXYBENZONE) LOTION [ZINKA, INC.]",
"spl_version": "7",
"published_date": "2025-11-17"
}
},
"productid": "52993-001_4354515e-3730-41be-e063-6294a90afc67",
"productndc": "52993-001",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE",
"proprietary_name": "Zinka Clear Zinc Oxide Sunscreen",
"active_ingred_unit": "mg/g; mg/g; mg/g; mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octinoxate, Zinc Oxide, Octisalate, Oxybenzone",
"start_marketing_date": "20070301",
"active_numerator_strength": "50; 30; 25; 43"
}Related drugs
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