hand sanitizer
Generic: ethyl alcohol
Labeler: ulineDrug Facts
Product Profile
Brand Name
hand sanitizer
Generic Name
ethyl alcohol
Labeler
uline
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
69790-770
Product ID
69790-770_4b09908e-c64c-c362-e063-6294a90ab66d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2016-03-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69790770
Hyphenated Format
69790-770
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
- 70 mL/100mL
Packaging
- 59 mL in 1 BOTTLE, PLASTIC (69790-770-16)
- 236 mL in 1 BOTTLE, PLASTIC (69790-770-34)
- 1999 mL in 1 BOTTLE, PLASTIC (69790-770-88)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4b09908e-c64c-c362-e063-6294a90ab66d", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["3bc9cfa2-2b1f-4892-93ff-cffa9f587804"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (69790-770-16)", "package_ndc": "69790-770-16", "marketing_start_date": "20160328"}, {"sample": false, "description": "236 mL in 1 BOTTLE, PLASTIC (69790-770-34)", "package_ndc": "69790-770-34", "marketing_start_date": "20160328"}, {"sample": false, "description": "1999 mL in 1 BOTTLE, PLASTIC (69790-770-88)", "package_ndc": "69790-770-88", "marketing_start_date": "20160328"}], "brand_name": "Hand Sanitizer", "product_id": "69790-770_4b09908e-c64c-c362-e063-6294a90ab66d", "dosage_form": "GEL", "product_ndc": "69790-770", "generic_name": "Ethyl Alcohol", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160328", "listing_expiration_date": "20271231"}