neosporin plus burn relief

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

Labeler: kenvue brands llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name neosporin plus burn relief
Generic Name bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride
Labeler kenvue brands llc
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

bacitracin zinc 500 [iU]/g, neomycin sulfate 3.5 mg/g, polymyxin b sulfate 10000 [iU]/g, pramoxine hydrochloride 10 mg/g

Manufacturer
Kenvue Brands LLC

Identifiers & Regulatory

Product NDC 69968-0518
Product ID 69968-0518_227889ba-a5e0-4b7c-e063-6294a90a73f6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M004
Listing Expiration 2026-12-31
Marketing Start 2019-02-01

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs] decreased cell wall synthesis & repair [pe] polymyxin-class antibacterial [epc] polymyxins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 699680518
Hyphenated Format 69968-0518

Supplemental Identifiers

RxCUI
1359350
UPC
0312547238366
UNII
89Y4M234ES 057Y626693 19371312D4 88AYB867L5

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name neosporin plus burn relief (source: ndc)
Generic Name bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride (source: ndc)
Application Number M004 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 500 [iU]/g
  • 3.5 mg/g
  • 10000 [iU]/g
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (69968-0518-1) / 14.2 g in 1 TUBE
source: ndc

Packages (1)

Ingredients (4)

bacitracin zinc (500 [iU]/g) neomycin sulfate (3.5 mg/g) polymyxin b sulfate (10000 [iU]/g) pramoxine hydrochloride (10 mg/g)

Linked Drug Pages (1)

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"}