cvs merthiolate
Generic: benzalkonium chloride
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
cvs merthiolate
Generic Name
benzalkonium chloride
Labeler
cvs pharmacy
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride 1.3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69842-749
Product ID
69842-749_0d19a0a5-ed0c-1796-e063-6294a90a7e8f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M003
Listing Expiration
2026-12-31
Marketing Start
2008-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69842749
Hyphenated Format
69842-749
Supplemental Identifiers
RxCUI
UPC
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
cvs merthiolate (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
M003 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.3 mg/mL
Packaging
- 59 mL in 1 BOTTLE, PLASTIC (69842-749-92)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0d19a0a5-ed0c-1796-e063-6294a90a7e8f", "openfda": {"upc": ["0050428266731"], "unii": ["F5UM2KM3W7"], "rxcui": ["1049254"], "spl_set_id": ["dd498ab1-8350-41aa-86fc-2db57005f3e2"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (69842-749-92)", "package_ndc": "69842-749-92", "marketing_start_date": "20080101"}], "brand_name": "CVS Merthiolate", "product_id": "69842-749_0d19a0a5-ed0c-1796-e063-6294a90a7e8f", "dosage_form": "LIQUID", "product_ndc": "69842-749", "generic_name": "Benzalkonium Chloride", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Merthiolate", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080101", "listing_expiration_date": "20261231"}