Package 62670-6701-0

Brand: anti bacterial hand gel sea and sandstone

Generic: alcohol
NDC Package

Package Facts

Identity

Package NDC 62670-6701-0
Digits Only 6267067010
Product NDC 62670-6701
Product ID 62670-6701_4c9bf5b8-83b9-f9f6-e063-6294a90a8559
Description

29 mL in 1 BOTTLE (62670-6701-0)

Marketing

Marketing Status
Marketed Since 2024-05-31
Brand anti bacterial hand gel sea and sandstone
Generic alcohol
Sample Package No

Linked Drug Pages (1)

Anti Bacterial Hand Gel Sea and Sandstone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4c9bf5b8-83b9-f9f6-e063-6294a90a8559", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["1bbaa2b3-9322-9aab-e063-6394a90a14c9"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (62670-6701-0)", "package_ndc": "62670-6701-0", "marketing_start_date": "20240531"}], "brand_name": "Anti Bacterial Hand Gel Sea and Sandstone", "product_id": "62670-6701_4c9bf5b8-83b9-f9f6-e063-6294a90a8559", "dosage_form": "GEL", "product_ndc": "62670-6701", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Bacterial Hand Gel", "brand_name_suffix": "Sea and Sandstone", "active_ingredients": [{"name": "ALCOHOL", "strength": "71 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240531", "listing_expiration_date": "20271231"}