Package 61010-8201-0

Brand: analgesic

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 61010-8201-0
Digits Only 6101082010
Product NDC 61010-8201
Product ID 61010-8201_10981167-c8a2-e068-e063-6394a90ab165
Description

.059 L in 1 BOTTLE, SPRAY (61010-8201-0)

Marketing

Marketing Status
Marketed Since 2018-09-01
Brand analgesic
Generic menthol
Sample Package No

Linked Drug Pages (1)

Analgesic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "10981167-c8a2-e068-e063-6394a90ab165", "openfda": {"upc": ["0780185001008"], "unii": ["L7T10EIP3A"], "spl_set_id": ["79e3b0e7-4ba5-4b9d-a980-5b6f18dba802"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".059 L in 1 BOTTLE, SPRAY (61010-8201-0)", "package_ndc": "61010-8201-0", "marketing_start_date": "20180901"}], "brand_name": "Analgesic", "product_id": "61010-8201_10981167-c8a2-e068-e063-6394a90ab165", "dosage_form": "SPRAY", "product_ndc": "61010-8201", "generic_name": "menthol", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Analgesic", "active_ingredients": [{"name": "MENTHOL", "strength": "70 mg/L"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180901", "listing_expiration_date": "20261231"}