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United States · US · US:24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d
PURPOSE
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBausch & Lomb Incorporated
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1124208001041 BOTTLE in 1 CARTON (24208-001-04) / 113 g in 1 BOTTLE
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": {
"3d7fe711-a671-df30-e063-6394a90afbbf": {
"match": "brand_token",
"title": "PURPOSE DUAL TREATMENT SPF 10 (OCTINOXATE 7.5%, OCTISALATE 5%, OXYBENZONE 3%) LOTION [ELYSIUM CONSUMER HEALTHCARE LLC]",
"spl_version": "1",
"published_date": "2025-09-05"
}
},
"productid": "24208-001_22f5cdc2-86cc-7dfd-e063-6394a90a539d",
"productndc": "24208-001",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; OXYBENZONE",
"proprietary_name": "PURPOSE",
"active_ingred_unit": "g/100g; g/100g; g/100g",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octinoxate, Octisalate and Oxybenzone",
"start_marketing_date": "20131007",
"active_numerator_strength": "7.5; 5; 3"
}Related drugs
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