alcohol
Generic: ethyl alcohol
Labeler: sam's west incDrug Facts
Product Profile
Brand Name
alcohol
Generic Name
ethyl alcohol
Labeler
sam's west inc
Dosage Form
LIQUID
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68196-602
Product ID
68196-602_1def0c4c-cef7-8ecd-e063-6394a90a0cac
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2024-07-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68196602
Hyphenated Format
68196-602
Supplemental Identifiers
RxCUI
UPC
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
alcohol (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
- 2000 mL in 1 BOTTLE, PLASTIC (68196-602-68)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1def0c4c-cef7-8ecd-e063-6394a90a0cac", "openfda": {"upc": ["0193968414573"], "unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["16625ecb-11c3-a097-e063-6294a90af3d5"], "manufacturer_name": ["Sam's West Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2000 mL in 1 BOTTLE, PLASTIC (68196-602-68)", "package_ndc": "68196-602-68", "marketing_start_date": "20240701"}], "brand_name": "Alcohol", "product_id": "68196-602_1def0c4c-cef7-8ecd-e063-6394a90a0cac", "dosage_form": "LIQUID", "product_ndc": "68196-602", "generic_name": "Ethyl Alcohol", "labeler_name": "Sam's West Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}