walgreens

Generic: ethyl alcohol

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name walgreens
Generic Name ethyl alcohol
Labeler walgreens
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol 700 mg/mL

Manufacturer
walgreens

Identifiers & Regulatory

Product NDC 0363-5721
Product ID 0363-5721_2d18c481-4be3-55ab-e063-6394a90a1f3c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2022-11-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03635721
Hyphenated Format 0363-5721

Supplemental Identifiers

RxCUI
581662
UNII
3K9958V90M

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 700 mg/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, PLASTIC (0363-5721-02)
source: ndc

Packages (1)

0363-5721-02 59 mL in 1 BOTTLE, PLASTIC (0363-5721-02)

Ingredients (1)

alcohol (700 mg/mL)

Linked Drug Pages (3)

Walgreens ndc-match (0.9) Walgreens ndc-match (0.9) Walgreens ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2d18c481-4be3-55ab-e063-6394a90a1f3c", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["ebf222f0-dc45-ee73-e053-2a95a90a0721"], "manufacturer_name": ["walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, PLASTIC (0363-5721-02)", "package_ndc": "0363-5721-02", "marketing_start_date": "20221102"}], "brand_name": "Walgreens", "product_id": "0363-5721_2d18c481-4be3-55ab-e063-6394a90a1f3c", "dosage_form": "GEL", "product_ndc": "0363-5721", "generic_name": "Ethyl Alcohol", "labeler_name": "walgreens", "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": "20221102", "listing_expiration_date": "20261231"}