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United States · US · US:10157-2106_bbba35d9-5dd7-4471-ad62-63061a9128a1
KANKA
UNIISPLATC C05AD
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBlistex Inc
CountryUS (United States)
ATC codeC05AD
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1110157210611 APPLICATOR in 1 BLISTER PACK (10157-2106-1) / 2 g in 1 APPLICATOR
- ndc1110157210622 APPLICATOR in 1 BLISTER PACK (10157-2106-2) / 2 g in 1 APPLICATOR
Annotations
UNII (FDA Substance ID)
U3RSY48JW5
BENZOCAINE
RxCUI 1399
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "U3RSY48JW5",
"rxcui": "1399",
"inchikey": "BLFLLBZGZJTVJG-UHFFFAOYSA-N",
"display_name": "BENZOCAINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"078fcdab-38a1-4a9a-bdd3-e17446591ea8": {
"match": "brand_token",
"title": "KANKA TRIPLE ACTION (BENZOCAINE AND MENTHOL, UNSPECIFIED FORM) GEL [BLISTEX INC.]",
"spl_version": "1",
"published_date": "2025-01-13"
}
},
"productid": "10157-2106_bbba35d9-5dd7-4471-ad62-63061a9128a1",
"productndc": "10157-2106",
"dosage_form": "GEL",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "BENZOCAINE; ZINC CHLORIDE",
"proprietary_name": "KANKA",
"active_ingred_unit": "mg/100g; g/100g",
"application_number": "M022",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Benzocaine and ZINC CHLORIDE",
"start_marketing_date": "20190925",
"active_numerator_strength": "20; .1"
}Related drugs
Other records sharing ATC code C05AD.
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