foamy blue
Generic: benzalkonium chloride
Labeler: pro chem solutions, inc.Drug Facts
Product Profile
Brand Name
foamy blue
Generic Name
benzalkonium chloride
Labeler
pro chem solutions, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
benzalkonium chloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
83188-405
Product ID
83188-405_34681507-5fc9-496f-e063-6394a90a51b5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2023-02-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83188405
Hyphenated Format
83188-405
Supplemental Identifiers
RxCUI
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
foamy blue (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1000 mL in 1 BAG (83188-405-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "34681507-5fc9-496f-e063-6394a90a51b5", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1233282"], "spl_set_id": ["aafecb36-082a-4577-a06a-4a5460e21a1d"], "manufacturer_name": ["Pro Chem Solutions, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (83188-405-04)", "package_ndc": "83188-405-04", "marketing_start_date": "20230210"}], "brand_name": "Foamy Blue", "product_id": "83188-405_34681507-5fc9-496f-e063-6394a90a51b5", "dosage_form": "SOLUTION", "product_ndc": "83188-405", "generic_name": "Benzalkonium Chloride", "labeler_name": "Pro Chem Solutions, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foamy Blue", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230210", "listing_expiration_date": "20261231"}