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United States · US · US:55681-017_4ee11cb5-7447-6745-e063-6394a90a5fbf
ProCure Zinc Oxide
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTwin Med LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11556810170128.3 g in 1 TUBE (55681-017-01)
- ndc11556810170256.6 g in 1 TUBE (55681-017-02)
- ndc115568101715425 g in 1 JAR (55681-017-15)
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": {
"3d848ec8-5197-6d39-e063-6394a90aaef6": {
"match": "brand_token",
"title": "PROCURE FOAMING HAND SANITIZER (ETHYL ALCOHOL 72%) GEL [TWIN MED LLC]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "55681-017_4ee11cb5-7447-6745-e063-6394a90a5fbf",
"productndc": "55681-017",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "ProCure Zinc Oxide",
"active_ingred_unit": "g/100g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide",
"start_marketing_date": "20250616",
"active_numerator_strength": "20"
}Access this data programmatically
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