walgreens
Generic: ethyl alcohol
Labeler: walgreenDrug Facts
Product Profile
Brand Name
walgreens
Generic Name
ethyl alcohol
Labeler
walgreen
Dosage Form
GEL
Routes
Active Ingredients
alcohol 700 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0363-5721
Product ID
0363-5721_3de70abd-512f-18aa-e063-6294a90a4acd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2022-10-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03635721
Hyphenated Format
0363-5721
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
walgreens (source: ndc)
Generic Name
ethyl alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 700 mg/mL
Packaging
- 59 mL in 1 BOTTLE, PLASTIC (0363-5721-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3de70abd-512f-18aa-e063-6294a90a4acd", "openfda": {"upc": ["0195602034550"], "unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["ebf222f0-dc46-ee73-e053-2a95a90a0721"], "manufacturer_name": ["Walgreen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (0363-5721-03)", "package_ndc": "0363-5721-03", "marketing_start_date": "20221019"}], "brand_name": "Walgreens", "product_id": "0363-5721_3de70abd-512f-18aa-e063-6294a90a4acd", "dosage_form": "GEL", "product_ndc": "0363-5721", "generic_name": "Ethyl Alcohol", "labeler_name": "Walgreen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Walgreens", "active_ingredients": [{"name": "ALCOHOL", "strength": "700 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221019", "listing_expiration_date": "20261231"}