Package 21749-706-89

Brand: purell advanced e3 rated instant hand sanitizer

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 21749-706-89
Digits Only 2174970689
Product NDC 21749-706
Product ID 21749-706_48374cc4-8a8b-ecd1-e063-6294a90ac363
Description

1200 mL in 1 BOTTLE (21749-706-89)

Marketing

Marketing Status
Marketed Since 2013-03-31
Brand purell advanced e3 rated instant hand sanitizer
Generic alcohol
Sample Package No

Linked Drug Pages (1)

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

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"}