🇺🇸
United States · US · US:84167-423_4e3d226b-57f2-75a6-e063-6394a90a96cd
APUREE Nailtific Extra-Max Strength Daytime Antigungal
UNIISPLATC D01AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGuangzhou Meixi Biotechnology Co., Ltd.
CountryUS (United States)
ATC codeD01AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1184167423011 VIAL, SINGLE-USE in 1 BOX (84167-423-01) / 30 LIQUID in 1 VIAL, SINGLE-USE
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": {
"521a0e40-a218-fabb-e063-6294a90ae9a2": {
"match": "brand_token",
"title": "APUREE PRO NAILTIFIC MAXIMUM STRENGTH DUAL-ACTION ANTIFUNGAL PEN LIQUID [GUANGZHOU MEIXI BIOTECHNOLOGY CO., LTD.]",
"spl_version": "1",
"published_date": "2026-05-20"
}
},
"productid": "84167-423_4e3d226b-57f2-75a6-e063-6394a90a96cd",
"productndc": "84167-423",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "TOLNAFTATE; UNDECYLENIC ACID",
"proprietary_name": "APUREE Nailtific Extra-Max Strength Daytime Antigungal",
"active_ingred_unit": "g/1; g/1",
"application_number": "M005",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "APUREE Nailtific Extra-Max Strength Daytime Antigungal",
"start_marketing_date": "20260330",
"active_numerator_strength": "1; 25"
}Related drugs
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