purell advanced soothing

Generic: alcohol

Labeler: gojo industries, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name purell advanced soothing
Generic Name alcohol
Labeler gojo industries, inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

alcohol .7 mL/mL

Manufacturer
GOJO Industries, Inc.

Identifiers & Regulatory

Product NDC 21749-713
Product ID 21749-713_28ff632a-64ae-011f-e063-6294a90a2c7a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2018-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21749713
Hyphenated Format 21749-713

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

Resolved Composition

Strengths
  • .7 mL/mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE (21749-713-02)
  • 118 mL in 1 PACKAGE (21749-713-04)
  • 236 mL in 1 BOTTLE (21749-713-08)
  • 295 mL in 1 PACKAGE (21749-713-10)
  • 354 mL in 1 BOTTLE (21749-713-12)
  • 710 mL in 1 PACKAGE (21749-713-24)
  • 1000 mL in 1 PACKAGE (21749-713-33)
  • 192 mL in 1 PACKAGE (21749-713-65)
source: ndc

Packages (8)

21749-713-02 59 mL in 1 BOTTLE (21749-713-02) 21749-713-04 118 mL in 1 PACKAGE (21749-713-04) 21749-713-08 236 mL in 1 BOTTLE (21749-713-08) 21749-713-10 295 mL in 1 PACKAGE (21749-713-10) 21749-713-12 354 mL in 1 BOTTLE (21749-713-12) 21749-713-24 710 mL in 1 PACKAGE (21749-713-24) 21749-713-33 1000 mL in 1 PACKAGE (21749-713-33) 21749-713-65 192 mL in 1 PACKAGE (21749-713-65)

Ingredients (1)

alcohol (.7 mL/mL)

Linked Drug Pages (1)

Purell Advanced Soothing ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "28ff632a-64ae-011f-e063-6294a90a2c7a", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["59b47629-8b4e-4084-8bc8-66c7e5599e9c"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE (21749-713-02)", "package_ndc": "21749-713-02", "marketing_start_date": "20181101"}, {"sample": false, "description": "118 mL in 1 PACKAGE (21749-713-04)", "package_ndc": "21749-713-04", "marketing_start_date": "20181101"}, {"sample": false, "description": "236 mL in 1 BOTTLE (21749-713-08)", "package_ndc": "21749-713-08", "marketing_start_date": "20181101"}, {"sample": false, "description": "295 mL in 1 PACKAGE (21749-713-10)", "package_ndc": "21749-713-10", "marketing_start_date": "20181101"}, {"sample": false, "description": "354 mL in 1 BOTTLE (21749-713-12)", "package_ndc": "21749-713-12", "marketing_start_date": "20181101"}, {"sample": false, "description": "710 mL in 1 PACKAGE (21749-713-24)", "package_ndc": "21749-713-24", "marketing_start_date": "20210801"}, {"sample": false, "description": "1000 mL in 1 PACKAGE (21749-713-33)", "package_ndc": "21749-713-33", "marketing_start_date": "20181101"}, {"sample": false, "description": "192 mL in 1 PACKAGE (21749-713-65)", "package_ndc": "21749-713-65", "marketing_start_date": "20210701"}], "brand_name": "Purell Advanced Soothing", "product_id": "21749-713_28ff632a-64ae-011f-e063-6294a90a2c7a", "dosage_form": "GEL", "product_ndc": "21749-713", "generic_name": "alcohol", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Purell Advanced Soothing", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}