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United States · US · US:73469-0619_fee7a27d-f2f9-4d6f-920e-7ba0d39a4bea
Tolnaftate Antifungal Powder
UNIISPLATC D01AE18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSCHOLL'S WELLNESS COMPANY LLC
CountryUS (United States)
ATC codeD01AE18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117346906194113 g in 1 BOTTLE (73469-0619-4)
Annotations
UNII (FDA Substance ID)
06KB629TKV
TOLNAFTATE
RxCUI 10637
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "06KB629TKV",
"rxcui": "10637",
"inchikey": "FUSNMLFNXJSCDI-UHFFFAOYSA-N",
"display_name": "TOLNAFTATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"af4ebb3b-041e-30dd-e053-2995a90a8d2d": {
"match": "brand_token",
"title": "TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [WAL-MART STORES, INC]",
"spl_version": "7",
"published_date": "2026-04-24"
}
},
"productid": "73469-0619_fee7a27d-f2f9-4d6f-920e-7ba0d39a4bea",
"productndc": "73469-0619",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TOLNAFTATE",
"proprietary_name": "Tolnaftate Antifungal Powder",
"active_ingred_unit": "g/100g",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Tolnaftate",
"start_marketing_date": "20251126",
"active_numerator_strength": "1"
}Related drugs
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