Package 69968-0518-1

Brand: neosporin plus burn relief

Generic: bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69968-0518-1
Digits Only 6996805181
Product NDC 69968-0518
Product ID 69968-0518_227889ba-a5e0-4b7c-e063-6294a90a73f6
Description

1 TUBE in 1 CARTON (69968-0518-1) / 14.2 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2019-02-01
Brand neosporin plus burn relief
Generic bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

NEOSPORIN Plus BURN RELIEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "227889ba-a5e0-4b7c-e063-6294a90a73f6", "openfda": {"upc": ["0312547238366"], "unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["3caa7fd1-bd66-427e-a6c0-1b137b205089"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69968-0518-1)  / 14.2 g in 1 TUBE", "package_ndc": "69968-0518-1", "marketing_start_date": "20190201"}], "brand_name": "NEOSPORIN Plus BURN RELIEF", "product_id": "69968-0518_227889ba-a5e0-4b7c-e063-6294a90a73f6", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "69968-0518", "generic_name": "Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NEOSPORIN Plus BURN RELIEF", "active_ingredients": [{"name": "BACITRACIN ZINC", "strength": "500 [iU]/g"}, {"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [iU]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190201", "listing_expiration_date": "20261231"}