pureforce

Generic: alcohol

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

Drug Facts

Product Profile

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

alcohol 534 mg/mL

Manufacturer
Ecolab Inc.

Identifiers & Regulatory

Product NDC 47593-498
Product ID 47593-498_1df566fc-164f-4a13-aeae-c0b7bb648dd0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2012-08-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47593498
Hyphenated Format 47593-498

Supplemental Identifiers

RxCUI
1039483
UPC
0780852000259
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 pureforce (source: ndc)
Generic Name alcohol (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 534 mg/mL
source: ndc
Packaging
  • 800 mL in 1 BAG (47593-498-25)
source: ndc

Packages (1)

Ingredients (1)

alcohol (534 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1df566fc-164f-4a13-aeae-c0b7bb648dd0", "openfda": {"upc": ["0780852000259"], "unii": ["3K9958V90M"], "rxcui": ["1039483"], "spl_set_id": ["775ee6e6-b3f8-4b97-b2b1-6f3a2defc696"], "manufacturer_name": ["Ecolab Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "800 mL in 1 BAG (47593-498-25)", "package_ndc": "47593-498-25", "marketing_start_date": "20120823"}], "brand_name": "PureForce", "product_id": "47593-498_1df566fc-164f-4a13-aeae-c0b7bb648dd0", "dosage_form": "SOLUTION", "product_ndc": "47593-498", "generic_name": "Alcohol", "labeler_name": "Ecolab Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PureForce", "active_ingredients": [{"name": "ALCOHOL", "strength": "534 mg/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120823", "listing_expiration_date": "20261231"}