Package 61010-1560-1

Brand: pain relieving

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 61010-1560-1
Digits Only 6101015601
Product NDC 61010-1560
Description

118.3 mL in 1 BOTTLE, SPRAY (61010-1560-1)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "10a94a5e-7097-232e-e063-6294a90a2c98", "openfda": {"upc": ["0780185001800"], "unii": ["L7T10EIP3A"], "rxcui": ["1086713"], "spl_set_id": ["df512ce6-ce1b-434d-9571-fb2e1d76e1d0"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118.3 mL in 1 BOTTLE, SPRAY (61010-1560-1)", "package_ndc": "61010-1560-1", "marketing_start_date": "20191007"}], "brand_name": "Pain Relieving", "product_id": "61010-1560_10a94a5e-7097-232e-e063-6294a90a2c98", "dosage_form": "SPRAY", "product_ndc": "61010-1560", "generic_name": "menthol, unspecified form", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relieving", "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"}