alcohol

Generic: alcohol

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

Drug Facts

Product Profile

Brand Name alcohol
Generic Name alcohol
Labeler uline
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol 62 mg/mL

Manufacturer
Uline

Identifiers & Regulatory

Product NDC 69790-849
Product ID 69790-849_4b09a991-ce1b-ead1-e063-6294a90afce2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2019-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69790849
Hyphenated Format 69790-849

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/mL
source: ndc
Packaging
  • 3785 mL in 1 BOTTLE, PLASTIC (69790-849-08)
  • 2082 mL in 1 DRUM (69790-849-55)
source: ndc

Packages (2)

69790-849-08 3785 mL in 1 BOTTLE, PLASTIC (69790-849-08) 69790-849-55 2082 mL in 1 DRUM (69790-849-55)

Ingredients (1)

alcohol (62 mg/mL)

Linked Drug Pages (1)

Alcohol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4b09a991-ce1b-ead1-e063-6294a90afce2", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["fdda41fa-d847-4cee-a070-91f0600b0fc8"], "manufacturer_name": ["Uline"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3785 mL in 1 BOTTLE, PLASTIC (69790-849-08)", "package_ndc": "69790-849-08", "marketing_start_date": "20190719"}, {"sample": false, "description": "2082 mL in 1 DRUM (69790-849-55)", "package_ndc": "69790-849-55", "marketing_start_date": "20200814"}], "brand_name": "Alcohol", "product_id": "69790-849_4b09a991-ce1b-ead1-e063-6294a90afce2", "dosage_form": "LIQUID", "product_ndc": "69790-849", "generic_name": "Alcohol", "labeler_name": "Uline", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alcohol", "active_ingredients": [{"name": "ALCOHOL", "strength": "62 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}