foaming hand

Generic: benzalkonium chloride

Labeler: cintas corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foaming hand
Generic Name benzalkonium chloride
Labeler cintas corporation
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1.3 mg/mL

Manufacturer
Cintas Corporation

Identifiers & Regulatory

Product NDC 42961-224
Product ID 42961-224_49dac8e8-231b-6f18-e063-6394a90aecd1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2020-07-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42961224
Hyphenated Format 42961-224

Supplemental Identifiers

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 foaming hand (source: ndc)
Generic Name benzalkonium chloride (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.3 mg/mL
source: ndc
Packaging
  • 800 mL in 1 BOTTLE, PUMP (42961-224-71)
source: ndc

Packages (1)

42961-224-71 800 mL in 1 BOTTLE, PUMP (42961-224-71)

Ingredients (1)

benzalkonium chloride (1.3 mg/mL)

Linked Drug Pages (1)

Foaming Hand ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "49dac8e8-231b-6f18-e063-6394a90aecd1", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["17fb34e7-c9e6-41aa-991f-bb54c84ed79c"], "manufacturer_name": ["Cintas Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "800 mL in 1 BOTTLE, PUMP (42961-224-71)", "package_ndc": "42961-224-71", "marketing_start_date": "20200720"}], "brand_name": "Foaming Hand", "product_id": "42961-224_49dac8e8-231b-6f18-e063-6394a90aecd1", "dosage_form": "LOTION", "product_ndc": "42961-224", "generic_name": "Benzalkonium Chloride", "labeler_name": "Cintas Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foaming Hand", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200720", "listing_expiration_date": "20271231"}