Package 21749-802-89

Brand: purell advanced e3 rated instant hand sanitizer foam

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 21749-802-89
Digits Only 2174980289
Product NDC 21749-802
Product ID 21749-802_2916dce7-fee4-552c-e063-6294a90a5cb5
Description

1200 mL in 1 BOTTLE (21749-802-89)

Marketing

Marketing Status
Marketed Since 2012-06-01
Brand purell advanced e3 rated instant hand sanitizer foam
Generic alcohol
Sample Package No

Linked Drug Pages (1)

PURELL Advanced E3 Rated Instant Hand Sanitizer Foam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2916dce7-fee4-552c-e063-6294a90a5cb5", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["616805"], "spl_set_id": ["1f78370b-132a-4759-8cbc-b5e093f90f8d"], "manufacturer_name": ["GOJO Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1200 mL in 1 BOTTLE (21749-802-89)", "package_ndc": "21749-802-89", "marketing_start_date": "20120601"}], "brand_name": "PURELL Advanced E3 Rated Instant Hand Sanitizer Foam", "product_id": "21749-802_2916dce7-fee4-552c-e063-6294a90a5cb5", "dosage_form": "LIQUID", "product_ndc": "21749-802", "generic_name": "alcohol", "labeler_name": "GOJO Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PURELL Advanced E3 Rated Instant Hand Sanitizer Foam", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120601", "listing_expiration_date": "20261231"}