fuzion ab foam

Generic: benzalkonium chloride

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

Drug Facts

Product Profile

Brand Name fuzion ab foam
Generic Name benzalkonium chloride
Labeler zep inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

benzalkonium chloride .13 g/100mL

Manufacturer
Zep Inc.

Identifiers & Regulatory

Product NDC 66949-111
Product ID 66949-111_46de4539-36b3-af75-e063-6294a90acfff
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2017-03-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66949111
Hyphenated Format 66949-111

Supplemental Identifiers

RxCUI
1046593
UNII
F5UM2KM3W7

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 fuzion ab foam (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .13 g/100mL
source: ndc
Packaging
  • 4800 mL in 1 CASE (66949-111-16)
source: ndc

Packages (1)

66949-111-16 4800 mL in 1 CASE (66949-111-16)

Ingredients (1)

benzalkonium chloride (.13 g/100mL)

Linked Drug Pages (1)

Fuzion AB Foam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "46de4539-36b3-af75-e063-6294a90acfff", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["b43ea64e-f7db-2250-e053-2995a90a43b3"], "manufacturer_name": ["Zep Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4800 mL in 1 CASE (66949-111-16)", "package_ndc": "66949-111-16", "marketing_start_date": "20170310"}], "brand_name": "Fuzion AB Foam", "product_id": "66949-111_46de4539-36b3-af75-e063-6294a90acfff", "dosage_form": "LIQUID", "product_ndc": "66949-111", "generic_name": "Benzalkonium Chloride", "labeler_name": "Zep Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fuzion AB Foam", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170310", "listing_expiration_date": "20261231"}