Package 72197-001-08

Brand: pharmacys prescription analgesic gel

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 72197-001-08
Digits Only 7219700108
Product NDC 72197-001
Product ID 72197-001_2c69ab76-e3d1-1436-e063-6294a90aa515
Description

227 g in 1 BOTTLE, PLASTIC (72197-001-08)

Marketing

Marketing Status
Marketed Since 2018-08-31
Brand pharmacys prescription analgesic gel
Generic menthol
Sample Package No

Linked Drug Pages (1)

Pharmacys Prescription Analgesic Gel ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2c69ab76-e3d1-1436-e063-6294a90aa515", "openfda": {"upc": ["0757437700057"], "unii": ["L7T10EIP3A"], "rxcui": ["1039043"], "spl_set_id": ["6f0725f2-833f-f3a0-e053-2a91aa0a3911"], "manufacturer_name": ["American Consumer Products Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE, PLASTIC (72197-001-08)", "package_ndc": "72197-001-08", "marketing_start_date": "20180831"}], "brand_name": "Pharmacys Prescription Analgesic Gel", "product_id": "72197-001_2c69ab76-e3d1-1436-e063-6294a90aa515", "dosage_form": "GEL", "product_ndc": "72197-001", "generic_name": "Menthol", "labeler_name": "American Consumer Products Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pharmacys Prescription Analgesic Gel", "active_ingredients": [{"name": "MENTHOL", "strength": "1 g/100g"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180831", "listing_expiration_date": "20261231"}