ethyl alcohol

Generic: alcohol

Labeler: asp global llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ethyl alcohol
Generic Name alcohol
Labeler asp global llc
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol 70 mL/100mL

Manufacturer
ASP Global LLC

Identifiers & Regulatory

Product NDC 59448-011
Product ID 59448-011_407eb059-1073-4a33-aaef-f964b4a98d87
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M003
Listing Expiration 2026-12-31
Marketing Start 2025-03-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59448011
Hyphenated Format 59448-011

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 ethyl alcohol (source: ndc)
Generic Name alcohol (source: ndc)
Application Number M003 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 70 mL/100mL
source: ndc
Packaging
  • 53 mL in 1 BOTTLE, PLASTIC (59448-011-01)
source: ndc

Packages (1)

Ingredients (1)

alcohol (70 mL/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "407eb059-1073-4a33-aaef-f964b4a98d87", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["67a4b949-ce8a-4841-a965-fcc94165135c"], "manufacturer_name": ["ASP Global LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "53 mL in 1 BOTTLE, PLASTIC (59448-011-01)", "package_ndc": "59448-011-01", "marketing_start_date": "20250401"}], "brand_name": "ETHYL ALCOHOL", "product_id": "59448-011_407eb059-1073-4a33-aaef-f964b4a98d87", "dosage_form": "GEL", "product_ndc": "59448-011", "generic_name": "ALCOHOL", "labeler_name": "ASP Global LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ETHYL ALCOHOL", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250302", "listing_expiration_date": "20261231"}