kay alcohol foam hand sanitizer
Generic: alcohol
Labeler: ecolab inc.Drug Facts
Product Profile
Brand Name
kay alcohol foam hand sanitizer
Generic Name
alcohol
Labeler
ecolab inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
47593-686
Product ID
47593-686_b4666fd9-8dfa-49fe-88d0-3bc2c4e43d62
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47593686
Hyphenated Format
47593-686
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
kay alcohol foam hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 1200 mL in 1 BOTTLE (47593-686-56)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "b4666fd9-8dfa-49fe-88d0-3bc2c4e43d62", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["616805"], "spl_set_id": ["37429e8a-581d-443e-8e8a-71fbb53c7c56"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 BOTTLE (47593-686-56)", "package_ndc": "47593-686-56", "marketing_start_date": "20251231"}], "brand_name": "Kay Alcohol Foam Hand Sanitizer", "product_id": "47593-686_b4666fd9-8dfa-49fe-88d0-3bc2c4e43d62", "dosage_form": "SOLUTION", "product_ndc": "47593-686", "generic_name": "Alcohol", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kay Alcohol Foam Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251231", "listing_expiration_date": "20261231"}