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United States · US · US:87184-899_43f13315-d6df-ef9e-e063-6294a90a310c
Absolut Skin Corticosoothe Anti-Itch
UNIISPLATC A07EA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAbsolut Skin Incorporated
CountryUS (United States)
ATC codeA07EA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1187184899001 TUBE in 1 BOX (87184-899-00) / 30 mL in 1 TUBE
Annotations
UNII (FDA Substance ID)
WI4X0X7BPJ
HYDROCORTISONE
RxCUI 5492
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WI4X0X7BPJ",
"rxcui": "5492",
"inchikey": "JYGXADMDTFJGBT-VWUMJDOOSA-N",
"display_name": "HYDROCORTISONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"3264543c-e8f5-da9a-e063-6394a90ac8c6": {
"match": "brand_token",
"title": "ABSOLUT SKIN SPF 50 MOISTURIZING SUNSCREEN (ETHYLHEXYL METHOXYCINNAMATE,ETHYLHEXYL SALICYLATE,METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL,OCTOCRYLENE) CREAM [GUANGZHOU TATA BIOTECHNOLOGY CO., LTD.]",
"spl_version": "3",
"published_date": "2025-12-23"
}
},
"productid": "87184-899_43f13315-d6df-ef9e-e063-6294a90a310c",
"productndc": "87184-899",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HYDROCORTISONE",
"proprietary_name": "Absolut Skin Corticosoothe Anti-Itch",
"active_ingred_unit": "mg/mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "HYDROCORTISONE",
"start_marketing_date": "20250912",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code A07EA02.
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