quickmend
Generic: benzethonium chloride
Labeler: equibal, inc.Drug Facts
Product Profile
Brand Name
quickmend
Generic Name
benzethonium chloride
Labeler
equibal, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzethonium chloride .09 mg/9mL
Manufacturer
Identifiers & Regulatory
Product NDC
53228-230
Product ID
53228-230_4633776e-e36a-88ee-e063-6294a90aab5b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2016-04-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53228230
Hyphenated Format
53228-230
Supplemental Identifiers
UNII
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
quickmend (source: ndc)
Generic Name
benzethonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .09 mg/9mL
Packaging
- 4.5 mL in 1 BOTTLE, PUMP (53228-230-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4633776e-e36a-88ee-e063-6294a90aab5b", "openfda": {"unii": ["PH41D05744"], "spl_set_id": ["9b0c85a4-9727-4940-a934-0b81a7c938cf"], "manufacturer_name": ["Equibal, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4.5 mL in 1 BOTTLE, PUMP (53228-230-02)", "package_ndc": "53228-230-02", "marketing_start_date": "20160401"}], "brand_name": "QuickMend", "product_id": "53228-230_4633776e-e36a-88ee-e063-6294a90aab5b", "dosage_form": "LIQUID", "product_ndc": "53228-230", "generic_name": "BENZETHONIUM CHLORIDE", "labeler_name": "Equibal, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QuickMend", "active_ingredients": [{"name": "BENZETHONIUM CHLORIDE", "strength": ".09 mg/9mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160401", "listing_expiration_date": "20261231"}