wipe those hands

Generic: benzalkonium chloride

Labeler: mighty good solutions, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name wipe those hands
Generic Name benzalkonium chloride
Labeler mighty good solutions, llc
Dosage Form CLOTH
Routes
TOPICAL
Active Ingredients

benzalkonium chloride 1.3 mg/mL

Manufacturer
Mighty Good Solutions, LLC

Identifiers & Regulatory

Product NDC 78091-251
Product ID 78091-251_408dfb29-a51b-70c7-e063-6294a90a949e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2023-07-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 78091251
Hyphenated Format 78091-251

Supplemental Identifiers

RxCUI
1038558
UPC
0850018852388 0850018852364 0850018852579 0850018852449 0850018852630
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 wipe those hands (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
  • 20 APPLICATOR in 1 POUCH (78091-251-02) / 4.05 mL in 1 APPLICATOR
  • 42 APPLICATOR in 1 POUCH (78091-251-03) / 4.05 mL in 1 APPLICATOR
  • 10 PACKET in 1 POUCH (78091-251-04) / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR
  • 30 PACKET in 1 POUCH (78091-251-05) / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR
  • 40 PACKET in 1 POUCH (78091-251-06) / 4.05 mL in 1 PACKET
source: ndc

Packages (5)

78091-251-02 20 APPLICATOR in 1 POUCH (78091-251-02) / 4.05 mL in 1 APPLICATOR 78091-251-03 42 APPLICATOR in 1 POUCH (78091-251-03) / 4.05 mL in 1 APPLICATOR 78091-251-04 10 PACKET in 1 POUCH (78091-251-04) / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR 78091-251-05 30 PACKET in 1 POUCH (78091-251-05) / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR 78091-251-06 40 PACKET in 1 POUCH (78091-251-06) / 4.05 mL in 1 PACKET

Ingredients (1)

benzalkonium chloride (1.3 mg/mL)

Linked Drug Pages (1)

Wipe Those Hands ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "408dfb29-a51b-70c7-e063-6294a90a949e", "openfda": {"upc": ["0850018852388", "0850018852364", "0850018852579", "0850018852449", "0850018852630"], "unii": ["F5UM2KM3W7"], "rxcui": ["1038558"], "spl_set_id": ["45b217ee-1524-4508-a18f-7db6a30d5169"], "manufacturer_name": ["Mighty Good Solutions, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 APPLICATOR in 1 POUCH (78091-251-02)  / 4.05 mL in 1 APPLICATOR", "package_ndc": "78091-251-02", "marketing_start_date": "20250402"}, {"sample": false, "description": "42 APPLICATOR in 1 POUCH (78091-251-03)  / 4.05 mL in 1 APPLICATOR", "package_ndc": "78091-251-03", "marketing_start_date": "20230715"}, {"sample": false, "description": "10 PACKET in 1 POUCH (78091-251-04)  / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR", "package_ndc": "78091-251-04", "marketing_start_date": "20230715"}, {"sample": false, "description": "30 PACKET in 1 POUCH (78091-251-05)  / 1 APPLICATOR in 1 PACKET / 4.05 mL in 1 APPLICATOR", "package_ndc": "78091-251-05", "marketing_start_date": "20230715"}, {"sample": false, "description": "40 PACKET in 1 POUCH (78091-251-06)  / 4.05 mL in 1 PACKET", "package_ndc": "78091-251-06", "marketing_start_date": "20230715"}], "brand_name": "Wipe Those Hands", "product_id": "78091-251_408dfb29-a51b-70c7-e063-6294a90a949e", "dosage_form": "CLOTH", "product_ndc": "78091-251", "generic_name": "BENZALKONIUM CHLORIDE", "labeler_name": "Mighty Good Solutions, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Wipe Those Hands", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230715", "listing_expiration_date": "20261231"}