Package 62670-6962-0

Brand: anti bacterial hand gel fiji white sands

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 62670-6962-0
Digits Only 6267069620
Product NDC 62670-6962
Product ID 62670-6962_46142cd2-e56c-8365-e063-6394a90a9d80
Description

29 mL in 1 BOTTLE (62670-6962-0)

Marketing

Marketing Status
Discontinued 2028-12-22
Brand anti bacterial hand gel fiji white sands
Generic alcohol
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "46142cd2-e56c-8365-e063-6394a90a9d80", "openfda": {"upc": ["0637293029175"], "unii": ["3K9958V90M"], "rxcui": ["2282911"], "spl_set_id": ["461420e0-a5b1-81df-e063-6394a90a94ec"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (62670-6962-0)", "package_ndc": "62670-6962-0", "marketing_end_date": "20281222", "marketing_start_date": "20251222"}], "brand_name": "Anti Bacterial Hand Gel Fiji White Sands", "product_id": "62670-6962_46142cd2-e56c-8365-e063-6394a90a9d80", "dosage_form": "GEL", "product_ndc": "62670-6962", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Bacterial Hand Gel", "brand_name_suffix": "Fiji White Sands", "active_ingredients": [{"name": "ALCOHOL", "strength": "71 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20281222", "marketing_start_date": "20251222"}