Package 62670-6937-0

Brand: anti bacterial hand gel pure wonder

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 62670-6937-0
Digits Only 6267069370
Product NDC 62670-6937
Product ID 62670-6937_468c8708-65b6-e471-e063-6394a90a0a99
Description

29 mL in 1 BOTTLE (62670-6937-0)

Marketing

Marketing Status
Discontinued 2028-10-20
Brand anti bacterial hand gel pure wonder
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Anti Bacterial Hand Gel Pure Wonder ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "468c8708-65b6-e471-e063-6394a90a0a99", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2282911"], "spl_set_id": ["468c90d7-3b9c-1641-e063-6394a90a928c"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (62670-6937-0)", "package_ndc": "62670-6937-0", "marketing_end_date": "20281020", "marketing_start_date": "20251020"}], "brand_name": "Anti Bacterial Hand Gel Pure Wonder", "product_id": "62670-6937_468c8708-65b6-e471-e063-6394a90a0a99", "dosage_form": "GEL", "product_ndc": "62670-6937", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Bacterial Hand Gel", "brand_name_suffix": "Pure Wonder", "active_ingredients": [{"name": "ALCOHOL", "strength": "71 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20281020", "marketing_start_date": "20251020"}