alcohol-free hand sanitizing foam

Generic: benzalkonium chloride

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

Drug Facts

Product Profile

Brand Name alcohol-free hand sanitizing foam
Generic Name benzalkonium chloride
Labeler united laboratories inc.
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1 mg/mL

Manufacturer
United Laboratories Inc.

Identifiers & Regulatory

Product NDC 63998-764
Product ID 63998-764_27c4d6fe-7567-073f-e063-6394a90afe9f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2019-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63998764
Hyphenated Format 63998-764

Supplemental Identifiers

RxCUI
1038799
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 alcohol-free hand sanitizing foam (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE (63998-764-01)
  • 750 mL in 1 BOTTLE (63998-764-02)
source: ndc

Packages (2)

63998-764-01 59 mL in 1 BOTTLE (63998-764-01) 63998-764-02 750 mL in 1 BOTTLE (63998-764-02)

Ingredients (1)

benzalkonium chloride (1 mg/mL)

Linked Drug Pages (1)

Alcohol-Free Hand Sanitizing Foam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "27c4d6fe-7567-073f-e063-6394a90afe9f", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1038799"], "spl_set_id": ["4f5ddead-1868-45c2-9657-762c9ca3a0e2"], "manufacturer_name": ["United Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE (63998-764-01)", "package_ndc": "63998-764-01", "marketing_start_date": "20190101"}, {"sample": false, "description": "750 mL in 1 BOTTLE (63998-764-02)", "package_ndc": "63998-764-02", "marketing_start_date": "20190101"}], "brand_name": "Alcohol-Free Hand Sanitizing Foam", "product_id": "63998-764_27c4d6fe-7567-073f-e063-6394a90afe9f", "dosage_form": "SOLUTION", "product_ndc": "63998-764", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "United Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol-Free Hand Sanitizing Foam", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}