Package 61010-1550-1

Brand: pain relieving roll-on

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 61010-1550-1
Digits Only 6101015501
Product NDC 61010-1550
Product ID 61010-1550_10a91ff8-4d59-15dd-e063-6394a90a3aad
Description

88 mL in 1 BOTTLE (61010-1550-1)

Marketing

Marketing Status
Marketed Since 2019-10-07
Brand pain relieving roll-on
Generic menthol, unspecified form
Sample Package No

Linked Drug Pages (1)

Pain Relieving Roll-On ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "10a91ff8-4d59-15dd-e063-6394a90a3aad", "openfda": {"upc": ["0780185001794"], "unii": ["L7T10EIP3A"], "rxcui": ["311509"], "spl_set_id": ["80118260-9c88-402d-9a90-ecfe62b4b54f"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (61010-1550-1)", "package_ndc": "61010-1550-1", "marketing_start_date": "20191007"}], "brand_name": "Pain Relieving Roll-On", "product_id": "61010-1550_10a91ff8-4d59-15dd-e063-6394a90a3aad", "dosage_form": "GEL", "product_ndc": "61010-1550", "generic_name": "menthol, unspecified form", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relieving Roll-On", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "7 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191007", "listing_expiration_date": "20261231"}