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United States · US · US:52358-0002_05e31db2-ee50-f735-e063-6394a90ae6f0
SUPRADERM
UNII
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOlen Skin Care Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc115235800021113 g in 1 JAR (52358-0002-1)
- ndc115235800022340 g in 1 JAR (52358-0002-2)
- ndc115235800023454 g in 1 JAR (52358-0002-3)
Annotations
UNII (FDA Substance ID)
7EV65EAW6H
LANOLIN
RxCUI 6227
Raw payload (JSON)
{
"unii": {
"unii": "7EV65EAW6H",
"rxcui": "6227",
"inchikey": null,
"display_name": "LANOLIN",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"productid": "52358-0002_05e31db2-ee50-f735-e063-6394a90ae6f0",
"productndc": "52358-0002",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LANOLIN; PETROLATUM",
"proprietary_name": "SUPRADERM",
"active_ingred_unit": "g/g; g/g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "white petrolatum, lanolin",
"start_marketing_date": "20141017",
"active_numerator_strength": ".15; .3"
}Access this data programmatically
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