purell advanced e3 rated instant hand sanitizer

Generic: alcohol

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

Drug Facts

Product Profile

Brand Name purell advanced e3 rated instant hand sanitizer
Generic Name alcohol
Labeler gojo industries, inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol .7 mL/mL

Manufacturer
GOJO Industries, Inc.

Identifiers & Regulatory

Product NDC 21749-706
Product ID 21749-706_48374cc4-8a8b-ecd1-e063-6294a90ac363
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2013-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21749706
Hyphenated Format 21749-706

Supplemental Identifiers

RxCUI
582753
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 e3 rated instant hand sanitizer (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
  • 1200 mL in 1 BOTTLE (21749-706-89)
source: ndc

Packages (1)

Ingredients (1)

alcohol (.7 mL/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48374cc4-8a8b-ecd1-e063-6294a90ac363", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["582753"], "spl_set_id": ["58adb1ba-73d8-4f6a-9296-269213e2f1e8"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 BOTTLE (21749-706-89)", "package_ndc": "21749-706-89", "marketing_start_date": "20130331"}], "brand_name": "PURELL Advanced E3 Rated Instant Hand Sanitizer", "product_id": "21749-706_48374cc4-8a8b-ecd1-e063-6294a90ac363", "dosage_form": "LIQUID", "product_ndc": "21749-706", "generic_name": "ALCOHOL", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PURELL Advanced E3 Rated Instant Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130331", "listing_expiration_date": "20271231"}