alcohol

Generic: alcohol

Labeler: aldi, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name alcohol
Generic Name alcohol
Labeler aldi, inc
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol 62 mg/100mL

Manufacturer
Aldi, Inc

Identifiers & Regulatory

Product NDC 64024-849
Product ID 64024-849_498c60b0-32a4-b619-e063-6294a90a7d59
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2020-12-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64024849
Hyphenated Format 64024-849

Supplemental Identifiers

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 alcohol (source: ndc)
Generic Name alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 62 mg/100mL
source: ndc
Packaging
  • 236 mL in 1 BOTTLE, PLASTIC (64024-849-34)
source: ndc

Packages (1)

64024-849-34 236 mL in 1 BOTTLE, PLASTIC (64024-849-34)

Ingredients (1)

alcohol (62 mg/100mL)

Linked Drug Pages (1)

Alcohol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "498c60b0-32a4-b619-e063-6294a90a7d59", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["aaa55815-ab6d-41c0-b04f-53de8001ebc7"], "manufacturer_name": ["Aldi, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, PLASTIC (64024-849-34)", "package_ndc": "64024-849-34", "marketing_start_date": "20201220"}], "brand_name": "Alcohol", "product_id": "64024-849_498c60b0-32a4-b619-e063-6294a90a7d59", "dosage_form": "LIQUID", "product_ndc": "64024-849", "generic_name": "Alcohol", "labeler_name": "Aldi, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mg/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201220", "listing_expiration_date": "20271231"}