ethyl alcohol
Generic: ethyl alcohol
Labeler: walmart inc.Drug Facts
Product Profile
Brand Name
ethyl alcohol
Generic Name
ethyl alcohol
Labeler
walmart inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol 62 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
49035-418
Product ID
49035-418_4bd2e99d-5e97-e02c-e063-6294a90a6555
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2019-12-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49035418
Hyphenated Format
49035-418
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
ethyl alcohol (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
- 29.5 mL in 1 PACKAGE (49035-418-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4bd2e99d-5e97-e02c-e063-6294a90a6555", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["f7d9bb83-0b80-458b-9554-8adbe51473e4"], "manufacturer_name": ["Walmart Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29.5 mL in 1 PACKAGE (49035-418-10)", "package_ndc": "49035-418-10", "marketing_start_date": "20191203"}], "brand_name": "Ethyl alcohol", "product_id": "49035-418_4bd2e99d-5e97-e02c-e063-6294a90a6555", "dosage_form": "GEL", "product_ndc": "49035-418", "generic_name": "Ethyl alcohol", "labeler_name": "Walmart Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ethyl alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191203", "listing_expiration_date": "20271231"}