instant hand sanitizer
Generic: alcohol
Labeler: henry schein, inc.Drug Facts
Product Profile
Brand Name
instant hand sanitizer
Generic Name
alcohol
Labeler
henry schein, inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol 665 mL/1000mL
Manufacturer
Identifiers & Regulatory
Product NDC
0404-5991
Product ID
0404-5991_2b5c3dc6-90bc-abe9-e063-6294a90af76e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2012-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04045991
Hyphenated Format
0404-5991
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
instant hand sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 665 mL/1000mL
Packaging
- 800 mL in 1 BOX (0404-5991-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2b5c3dc6-90bc-abe9-e063-6294a90af76e", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["616762"], "spl_set_id": ["e80feb63-2c51-4164-806d-778e39e620e8"], "manufacturer_name": ["Henry Schein, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "800 mL in 1 BOX (0404-5991-01)", "package_ndc": "0404-5991-01", "marketing_start_date": "20120201"}], "brand_name": "Instant Hand Sanitizer", "product_id": "0404-5991_2b5c3dc6-90bc-abe9-e063-6294a90af76e", "dosage_form": "GEL", "product_ndc": "0404-5991", "generic_name": "alcohol", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Instant Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "665 mL/1000mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120201", "listing_expiration_date": "20261231"}