hand sanitizer
Generic: ethyl alcohol
Labeler: innovation specialties incDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
ethyl alcohol
Labeler
innovation specialties inc
Dosage Form
GEL
Routes
Active Ingredients
alcohol 62 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
76138-114
Product ID
76138-114_1cee8656-3017-15b2-e063-6394a90a1e1d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2016-01-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76138114
Hyphenated Format
76138-114
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
ethyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 62 mL/100mL
Packaging
- 30 mL in 1 BOTTLE (76138-114-13)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1cee8656-3017-15b2-e063-6394a90a1e1d", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["b2eee632-5a1d-4df5-99c8-8ceb3d644c94"], "manufacturer_name": ["Innovation Specialties Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (76138-114-13)", "package_ndc": "76138-114-13", "marketing_start_date": "20160102"}], "brand_name": "Hand Sanitizer", "product_id": "76138-114_1cee8656-3017-15b2-e063-6394a90a1e1d", "dosage_form": "GEL", "product_ndc": "76138-114", "generic_name": "Ethyl alcohol", "labeler_name": "Innovation Specialties Inc", "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": "20160102", "listing_expiration_date": "20261231"}