facilipro

Generic: ethyl alcohol

Labeler: ecolab inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name facilipro
Generic Name ethyl alcohol
Labeler ecolab inc.
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

alcohol 620 mg/mL

Manufacturer
Ecolab Inc.

Identifiers & Regulatory

Product NDC 47593-563
Product ID 47593-563_fb764b9a-7e55-47eb-a4f2-437e2fcfb129
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2010-12-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47593563
Hyphenated Format 47593-563

Supplemental Identifiers

RxCUI
247835
UPC
0025469012586
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 facilipro (source: ndc)
Generic Name ethyl alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 620 mg/mL
source: ndc
Packaging
  • 1200 mL in 1 BOTTLE, PLASTIC (47593-563-56)
source: ndc

Packages (1)

47593-563-56 1200 mL in 1 BOTTLE, PLASTIC (47593-563-56)

Ingredients (1)

alcohol (620 mg/mL)

Linked Drug Pages (1)

Facilipro ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "fb764b9a-7e55-47eb-a4f2-437e2fcfb129", "openfda": {"upc": ["0025469012586"], "unii": ["3K9958V90M"], "rxcui": ["247835"], "spl_set_id": ["71f2504a-2da3-4273-9603-47e4cf64ad24"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 BOTTLE, PLASTIC (47593-563-56)", "package_ndc": "47593-563-56", "marketing_start_date": "20101203"}], "brand_name": "Facilipro", "product_id": "47593-563_fb764b9a-7e55-47eb-a4f2-437e2fcfb129", "dosage_form": "SOLUTION", "product_ndc": "47593-563", "generic_name": "Ethyl Alcohol", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Facilipro", "active_ingredients": [{"name": "ALCOHOL", "strength": "620 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20101203", "listing_expiration_date": "20261231"}