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United States · US · US:67777-223_4f5b6507-0292-edc3-e063-6294a90a3c79
Zinc Oxide
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDynarex Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11677772230272 BOX in 1 CASE (67777-223-02) / 1 TUBE in 1 BOX (67777-223-11) / 28.4 g in 1 TUBE (67777-223-01)
- ndc11677772230472 BOX in 1 CASE (67777-223-04) / 1 TUBE in 1 BOX (67777-223-13) / 56.7 g in 1 TUBE (67777-223-03)
- ndc11677772230612 JAR in 1 CASE (67777-223-06) / 425 g in 1 JAR (67777-223-05)
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": {
"63b551fc-7d16-c099-e053-2a91aa0a5f2c": {
"match": "brand_token",
"title": "ZINC OXIDE 20% (ZINC OXIDE) OINTMENT [TRIFECTA PHARMACEUTICALS USA]",
"spl_version": "7",
"published_date": "2026-05-20"
}
},
"productid": "67777-223_4f5b6507-0292-edc3-e063-6294a90a3c79",
"productndc": "67777-223",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ZINC OXIDE",
"proprietary_name": "Zinc Oxide",
"active_ingred_unit": "mg/g",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Zinc Oxide Ointment",
"start_marketing_date": "20240229",
"active_numerator_strength": "200"
}Access this data programmatically
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