blistex foille medicated first aid
Generic: benzocaine and chloroxylenol
Labeler: blistex inc.Drug Facts
Product Profile
Brand Name
blistex foille medicated first aid
Generic Name
benzocaine and chloroxylenol
Labeler
blistex inc.
Dosage Form
OINTMENT
Routes
Active Ingredients
benzocaine 5 g/100g, chloroxylenol .1 g/100g
Manufacturer
Identifiers & Regulatory
Product NDC
10157-9302
Product ID
10157-9302_78fbbd4f-548d-4b5a-8e15-2ae2a01a3592
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2013-03-05
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
101579302
Hyphenated Format
10157-9302
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
blistex foille medicated first aid (source: ndc)
Generic Name
benzocaine and chloroxylenol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100g
- .1 g/100g
Packaging
- 1 TUBE in 1 CARTON (10157-9302-3) / 14 g in 1 TUBE
- 1 TUBE in 1 CARTON (10157-9302-4) / 28 g in 1 TUBE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "78fbbd4f-548d-4b5a-8e15-2ae2a01a3592", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["0041388003023"], "unii": ["U3RSY48JW5", "0F32U78V2Q"], "rxcui": ["199005", "213034"], "spl_set_id": ["e2eca808-e97b-43e0-aa51-7025cc61c7a8"], "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 (10157-9302-3) / 14 g in 1 TUBE", "package_ndc": "10157-9302-3", "marketing_start_date": "20160923"}, {"sample": false, "description": "1 TUBE in 1 CARTON (10157-9302-4) / 28 g in 1 TUBE", "package_ndc": "10157-9302-4", "marketing_start_date": "20130305"}], "brand_name": "Blistex Foille Medicated First Aid", "product_id": "10157-9302_78fbbd4f-548d-4b5a-8e15-2ae2a01a3592", "dosage_form": "OINTMENT", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "10157-9302", "generic_name": "Benzocaine and Chloroxylenol", "labeler_name": "Blistex Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Blistex", "brand_name_suffix": "Foille Medicated First Aid", "active_ingredients": [{"name": "BENZOCAINE", "strength": "5 g/100g"}, {"name": "CHLOROXYLENOL", "strength": ".1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130305", "listing_expiration_date": "20261231"}