Package 62670-6881-0

Brand: anti bacterial hand gel firecracker pop

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 62670-6881-0
Digits Only 6267068810
Product NDC 62670-6881
Product ID 62670-6881_38e226d8-5ef2-e23d-e063-6394a90a80b1
Description

29 mL in 1 BOTTLE (62670-6881-0)

Marketing

Marketing Status
Discontinued 2028-05-05
Brand anti bacterial hand gel firecracker pop
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Anti Bacterial Hand Gel Firecracker Pop ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "38e226d8-5ef2-e23d-e063-6394a90a80b1", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["2282911"], "spl_set_id": ["38e21dcc-ea88-c6cd-e063-6294a90a057e"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (62670-6881-0)", "package_ndc": "62670-6881-0", "marketing_end_date": "20280505", "marketing_start_date": "20250505"}], "brand_name": "Anti Bacterial Hand Gel Firecracker Pop", "product_id": "62670-6881_38e226d8-5ef2-e23d-e063-6394a90a80b1", "dosage_form": "GEL", "product_ndc": "62670-6881", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Bacterial Hand Gel", "brand_name_suffix": "Firecracker Pop", "active_ingredients": [{"name": "ALCOHOL", "strength": "71 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280505", "marketing_start_date": "20250505"}