Package 61010-8200-1

Brand: analgesic

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 61010-8200-1
Digits Only 6101082001
Product NDC 61010-8200
Description

118 mL in 1 BOTTLE, SPRAY (61010-8200-1)

Marketing

Marketing Status
Marketed Since 2011-10-26
Brand analgesic
Generic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "12b7defb-8710-5fd7-e063-6294a90a8a03", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["1086713"], "spl_set_id": ["b0f4010c-995f-40e1-aa40-92760e697a61"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE, SPRAY (61010-8200-1)", "package_ndc": "61010-8200-1", "marketing_start_date": "20111026"}], "brand_name": "Analgesic", "product_id": "61010-8200_12b7defb-8710-5fd7-e063-6294a90a8a03", "dosage_form": "SPRAY", "product_ndc": "61010-8200", "generic_name": "menthol", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Analgesic", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "70 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20111026", "listing_expiration_date": "20261231"}