kank-a mouth pain

Generic: benzocaine

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

Drug Facts

Product Profile

Brand Name kank-a mouth pain
Generic Name benzocaine
Labeler blistex inc.
Dosage Form LIQUID
Routes
BUCCAL
Active Ingredients

benzocaine 200 mg/mL

Manufacturer
Blistex Inc.

Identifiers & Regulatory

Product NDC 10157-9477
Product ID 10157-9477_55568382-5b9f-4bc1-9532-38fb810532d3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2011-12-01

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 101579477
Hyphenated Format 10157-9477

Supplemental Identifiers

RxCUI
308657
UPC
0041388203911
UNII
U3RSY48JW5
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 kank-a mouth pain (source: ndc)
Generic Name benzocaine (source: ndc)
Application Number M022 (source: ndc)
Routes
BUCCAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/mL
source: ndc
Packaging
  • 9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1)
source: ndc

Packages (1)

Ingredients (1)

benzocaine (200 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["BUCCAL"], "spl_id": "55568382-5b9f-4bc1-9532-38fb810532d3", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["0041388203911"], "unii": ["U3RSY48JW5"], "rxcui": ["308657"], "spl_set_id": ["eebc03ba-f849-4e70-a653-834f383b6aa4"], "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": "9.75 mL in 1 BOTTLE, WITH APPLICATOR (10157-9477-1)", "package_ndc": "10157-9477-1", "marketing_start_date": "20111201"}], "brand_name": "Kank-A Mouth Pain", "product_id": "10157-9477_55568382-5b9f-4bc1-9532-38fb810532d3", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "10157-9477", "generic_name": "Benzocaine", "labeler_name": "Blistex Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kank-A", "brand_name_suffix": "Mouth Pain", "active_ingredients": [{"name": "BENZOCAINE", "strength": "200 mg/mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20111201", "listing_expiration_date": "20261231"}