hand wash
Generic: benzalkonium chloride
Labeler: meijer, inc.Drug Facts
Product Profile
Brand Name
hand wash
Generic Name
benzalkonium chloride
Labeler
meijer, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
benzalkonium chloride 1.3 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
41250-661
Product ID
41250-661_4b33dcaa-f3c2-467e-e063-6294a90a4e16
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2019-12-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
41250661
Hyphenated Format
41250-661
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
hand wash (source: ndc)
Generic Name
benzalkonium chloride (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.3 mg/mL
Packaging
- 221 mL in 1 BOTTLE, PUMP (41250-661-96)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b33dcaa-f3c2-467e-e063-6294a90a4e16", "openfda": {"unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["8fbbc798-ac00-4755-a2c2-5cd5b5c01ae4"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "221 mL in 1 BOTTLE, PUMP (41250-661-96)", "package_ndc": "41250-661-96", "marketing_start_date": "20191220"}], "brand_name": "Hand Wash", "product_id": "41250-661_4b33dcaa-f3c2-467e-e063-6294a90a4e16", "dosage_form": "LIQUID", "product_ndc": "41250-661", "generic_name": "Benzalkonium chloride", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Wash", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191220", "listing_expiration_date": "20271231"}