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United States · US · US:55505-177_29be9a78-384b-4807-ab8b-1417d6e0e48f
Fungi Nail Toe and Foot
UNIISPLATC D01AE18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKramer Laboratories
CountryUS (United States)
ATC codeD01AE18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1155505177241 BOTTLE, WITH APPLICATOR in 1 CARTON (55505-177-24) / 15 mL in 1 BOTTLE, WITH APPLICATOR
- ndc1155505177261 BOTTLE, WITH APPLICATOR in 1 CARTON (55505-177-26) / 30 mL in 1 BOTTLE, WITH APPLICATOR
- ndc1155505177801 BOTTLE, SPRAY in 1 CARTON (55505-177-80) / 30 mL in 1 BOTTLE, SPRAY
- ndc1155505177872 CARTON in 1 PACKAGE (55505-177-87) / 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR
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": {
"e21ccb83-54ff-4605-80bf-7b4b789c7cb7": {
"match": "brand_token",
"title": "FUNGI NAIL TOE AND FOOT (TOLNAFTATE) OINTMENT [KRAMER LABORATORIES]",
"spl_version": "11",
"published_date": "2026-03-24"
}
},
"productid": "55505-177_29be9a78-384b-4807-ab8b-1417d6e0e48f",
"productndc": "55505-177",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TOLNAFTATE",
"proprietary_name": "Fungi Nail Toe and Foot",
"active_ingred_unit": "mg/mL",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Tolnaftate",
"start_marketing_date": "20190325",
"active_numerator_strength": "10"
}Related drugs
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