Package 50241-339-02

Brand: mg dermafoam

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 50241-339-02
Digits Only 5024133902
Product NDC 50241-339
Description

1 BOTTLE, PLASTIC in 1 BOX (50241-339-02) / 3.80564 kg in 1 BOTTLE, PLASTIC (50241-339-01)

Marketing

Marketing Status
Marketed Since 2018-09-25
Brand mg dermafoam
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1fe4feed-fa93-403a-b759-a6b2d0274961", "openfda": {"unii": ["F5UM2KM3W7"], "spl_set_id": ["4a43a605-f333-4c76-a476-476a9cc2e13a"], "manufacturer_name": ["Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (50241-339-02)  / 3.80564 kg in 1 BOTTLE, PLASTIC (50241-339-01)", "package_ndc": "50241-339-02", "marketing_start_date": "20180925"}], "brand_name": "MG DermaFoam", "product_id": "50241-339_1fe4feed-fa93-403a-b759-a6b2d0274961", "dosage_form": "LIQUID", "product_ndc": "50241-339", "generic_name": "Benzalkonium Chloride", "labeler_name": "Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MG DermaFoam", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "13 kg/100kg"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180925", "listing_expiration_date": "20261231"}