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United States Β· US Β· US:84047-2090_42f4dd42-3e3b-36ab-e063-6294a90a91ed
Refy Skin Trio
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRefy
CountryUS (United States)
ATC codeβ
Dispensingβ
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs Β· 1
- ndc1184047209021 BOTTLE in 1 CARTON (84047-2090-2) / 36 mL in 1 BOTTLE (84047-2090-1)
Annotations
UNII (FDA Substance ID)
SOI2LOH54Z
ZINC OXIDE
RxCUI 11423
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "SOI2LOH54Z",
"rxcui": "11423",
"inchikey": "RNWHGQJWIACOKP-UHFFFAOYSA-N",
"display_name": "ZINC OXIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"3029a690-dbb0-ff15-e063-6394a90abdbe": {
"match": "brand_token",
"title": "REFY SKIN TRIO (ZINC OXIDE) LOTION [REFY]",
"spl_version": "3",
"published_date": "2025-11-17"
}
},
"productid": "84047-2090_42f4dd42-3e3b-36ab-e063-6294a90a91ed",
"productndc": "84047-2090",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Refy Skin Trio",
"active_ingred_unit": "mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide",
"start_marketing_date": "20240329",
"active_numerator_strength": "154"
}Access this data programmatically
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