hand sanitizer
Generic: alcohol
Labeler: custom chemical solutionsDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
alcohol
Labeler
custom chemical solutions
Dosage Form
GEL
Routes
Active Ingredients
alcohol 62 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
77955-001
Product ID
77955-001_0f8c444d-e0e1-3155-e063-6394a90a55df
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-06-11
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
77955001
Hyphenated Format
77955-001
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 sanitizer (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 62 mL/100mL
Packaging
- 1000 mL in 1 BOTTLE (77955-001-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0f8c444d-e0e1-3155-e063-6394a90a55df", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["a7c07167-b27b-8217-e053-2995a90ac541"], "manufacturer_name": ["Custom Chemical Solutions"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BOTTLE (77955-001-02)", "package_ndc": "77955-001-02", "marketing_start_date": "20200611"}], "brand_name": "Hand Sanitizer", "product_id": "77955-001_0f8c444d-e0e1-3155-e063-6394a90a55df", "dosage_form": "GEL", "product_ndc": "77955-001", "generic_name": "Alcohol", "labeler_name": "Custom Chemical Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200611", "listing_expiration_date": "20261231"}