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United States · US · US:11523-0011_48850bbc-9ec2-b7ee-e063-6394a90a9f0d
Lotrimin Daily Prevention
UNIISPLATC D01AE18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBayer HealthCare LLC.
CountryUS (United States)
ATC codeD01AE18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11115230011190 g in 1 BOTTLE (11523-0011-1)
- ndc11115230011228 g in 1 BOTTLE (11523-0011-2)
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": {
"cebd222c-074f-443c-bd37-612114b27bbd": {
"match": "brand_token",
"title": "LOTRIMIN ANTIFUNGAL (MICONAZOLE NITRATE) POWDER [BAYER HEALTHCARE LLC.]",
"spl_version": "10",
"published_date": "2026-01-19"
}
},
"productid": "11523-0011_48850bbc-9ec2-b7ee-e063-6394a90a9f0d",
"productndc": "11523-0011",
"dosage_form": "POWDER",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TOLNAFTATE",
"proprietary_name": "Lotrimin Daily Prevention",
"active_ingred_unit": "mg/g",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "tolnaftate",
"start_marketing_date": "20200214",
"active_numerator_strength": "10"
}Related drugs
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Access this data programmatically
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