kanka triple action

Generic: benzocaine and menthol, unspecified form

Labeler: blistex inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name kanka triple action
Generic Name benzocaine and menthol, unspecified form
Labeler blistex inc.
Dosage Form GEL
Routes
ORAL
Active Ingredients

benzocaine 20 g/100g, menthol, unspecified form 2 g/100g

Manufacturer
Blistex Inc.

Identifiers & Regulatory

Product NDC 10157-2127
Product ID 10157-2127_225703ba-c471-4c9a-9c01-4b7f075b7878
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2025-01-06

Pharmacologic Class

Established (EPC)
standardized chemical allergen [epc]
Chemical Structure
allergens [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 101572127
Hyphenated Format 10157-2127

Supplemental Identifiers

RxCUI
1006079
UPC
0041388013145
UNII
U3RSY48JW5 L7T10EIP3A
NUI
N0000185508 N0000175629 N0000184306 M0000728

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name kanka triple action (source: ndc)
Generic Name benzocaine and menthol, unspecified form (source: ndc)
Application Number M022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 g/100g
  • 2 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBE
source: ndc

Packages (1)

10157-2127-1 1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBE

Ingredients (2)

benzocaine (20 g/100g) menthol, unspecified form (2 g/100g)

Linked Drug Pages (1)

Kanka Triple Action ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "225703ba-c471-4c9a-9c01-4b7f075b7878", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["0041388013145"], "unii": ["U3RSY48JW5", "L7T10EIP3A"], "rxcui": ["1006079"], "spl_set_id": ["078fcdab-38a1-4a9a-bdd3-e17446591ea8"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Blistex Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10157-2127-1)  / 11.9 g in 1 TUBE", "package_ndc": "10157-2127-1", "marketing_start_date": "20250106"}], "brand_name": "Kanka Triple Action", "product_id": "10157-2127_225703ba-c471-4c9a-9c01-4b7f075b7878", "dosage_form": "GEL", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "10157-2127", "generic_name": "BENZOCAINE and MENTHOL, UNSPECIFIED FORM", "labeler_name": "Blistex Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kanka Triple Action", "active_ingredients": [{"name": "BENZOCAINE", "strength": "20 g/100g"}, {"name": "MENTHOL, UNSPECIFIED FORM", "strength": "2 g/100g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250106", "listing_expiration_date": "20261231"}