Package 79481-0610-9

Brand: 4x medicated severe toothache and gum gel

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 79481-0610-9
Digits Only 7948106109
Product NDC 79481-0610
Description

1 TUBE in 1 CARTON (79481-0610-9) / 7 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-11-20
Brand 4x medicated severe toothache and gum gel
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437fd357-4fcb-b91b-e063-6394a90a2f3e", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["0713733254823"], "unii": ["F5UM2KM3W7", "U3RSY48JW5", "L7T10EIP3A", "86Q357L16B"], "rxcui": ["2369638"], "spl_set_id": ["97ce7890-5093-1763-e053-2a95a90afae7"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (79481-0610-9)  / 7 g in 1 TUBE", "package_ndc": "79481-0610-9", "marketing_start_date": "20191120"}], "brand_name": "4x Medicated Severe Toothache and Gum Gel", "product_id": "79481-0610_437fd357-4fcb-b91b-e063-6394a90a2f3e", "dosage_form": "GEL", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "79481-0610", "generic_name": "Benzalkonium chloride", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "4x Medicated Severe Toothache and Gum Gel", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": ".13 g/100g"}, {"name": "BENZOCAINE", "strength": "20 g/100g"}, {"name": "MENTHOL", "strength": ".5 g/100g"}, {"name": "ZINC CHLORIDE", "strength": ".15 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191120", "listing_expiration_date": "20261231"}