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United States · US · US:60232-0008_c9d33e9b-77bd-4ca7-b228-f49318307a70
Private Label Super Light Oil-Free SPF45
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSwiss-American CDMO, LLC
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11602320008260 g in 1 BOTTLE (60232-0008-2)
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": {
"e74bddea-c1ac-4e4e-84bd-5a9defb85b2d": {
"match": "brand_token",
"title": "PRIVATE LABEL ANTIFUNGAL BARRIER CREAM (2% MICONAZOLE NITRATE CREAM) CREAM [SWISS-AMERICAN CDMO, LLC]",
"spl_version": "4",
"published_date": "2026-01-09"
}
},
"productid": "60232-0008_c9d33e9b-77bd-4ca7-b228-f49318307a70",
"productndc": "60232-0008",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; ZINC OXIDE",
"proprietary_name": "Private Label Super Light Oil-Free SPF45",
"active_ingred_unit": "g/1000g; g/1000g; g/1000g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "2.75% Octinsalate, 7.50% Octinoxate, 8.00% Zinc Oxide Sunscreen",
"start_marketing_date": "20110322",
"active_numerator_strength": "75; 27.5; 80"
}Related drugs
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