Package 62670-6790-0

Brand: Anti-BacterialHandSpray Eucalyptus and Spearmint

Generic: Alcohol
NDC Package

Package Facts

Identity

Package NDC 62670-6790-0
Digits Only 6267067900
Product NDC 62670-6790
Description

29 mL in 1 BOTTLE, SPRAY (62670-6790-0)

Marketing

Marketing Status
Discontinued 2027-08-26
Brand Anti-BacterialHandSpray Eucalyptus and Spearmint
Generic Alcohol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "29a376e5-675c-b0b0-e063-6394a90a68c0", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["1425407"], "spl_set_id": ["29a37aad-c6d2-b174-e063-6394a90abc3e"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE, SPRAY (62670-6790-0)", "package_ndc": "62670-6790-0", "marketing_end_date": "20270826", "marketing_start_date": "20240826"}], "brand_name": "Anti-BacterialHandSpray Eucalyptus and Spearmint", "product_id": "62670-6790_29a376e5-675c-b0b0-e063-6394a90a68c0", "dosage_form": "SPRAY", "product_ndc": "62670-6790", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti-BacterialHandSpray", "brand_name_suffix": "Eucalyptus and Spearmint", "active_ingredients": [{"name": "ALCOHOL", "strength": "72 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270826", "marketing_start_date": "20240826"}