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United States · US · US:69367-247_33621d74-84ee-4831-8935-95cd618398fc
SODIUM SULFACETAMIDE, SULFUR
UNIISPLATC D10AF
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWestminster Pharmaceuticals, LLC
CountryUS (United States)
ATC codeD10AF
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116936724706170.3 g in 1 BOTTLE (69367-247-06)
- ndc116936724708227 g in 1 BOTTLE (69367-247-08)
- ndc116936724712340.2 g in 1 BOTTLE (69367-247-12)
Annotations
UNII (FDA Substance ID)
4NRT660KJQ
SULFACETAMIDE SODIUM
RxCUI 82101
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4NRT660KJQ",
"rxcui": "82101",
"inchikey": "IHCDKJZZFOUARO-UHFFFAOYSA-M",
"display_name": "SULFACETAMIDE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"52430b12-4d5f-d1e1-e063-6394a90abd64": {
"match": "brand_token",
"title": "SODIUM FLUORIDE RINSE LIQUID [ROCKLAND COSMETICS, INC.]",
"spl_version": "1",
"published_date": "2026-05-21"
}
},
"productid": "69367-247_33621d74-84ee-4831-8935-95cd618398fc",
"productndc": "69367-247",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SULFACETAMIDE SODIUM; SULFUR",
"proprietary_name": "SODIUM SULFACETAMIDE, SULFUR",
"active_ingred_unit": "mg/g; mg/g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "sulfacetamide sodium and sulfur",
"start_marketing_date": "20200505",
"active_numerator_strength": "100; 50"
}Related drugs
Other records sharing ATC code D10AF.
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