sunmark triple antibiotic plus pain relief

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

Labeler: a-s medication solutions
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sunmark triple antibiotic plus pain relief
Generic Name polymyxin b sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
Labeler a-s medication solutions
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
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6172
Product ID 50090-6172_8ccae7c4-e443-4cec-a31d-764334293b65
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M004
Marketing Start 2012-03-31
Marketing End 2027-08-31

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 500906172
Hyphenated Format 50090-6172

Supplemental Identifiers

RxCUI
1359350
UNII
89Y4M234ES 057Y626693 19371312D4 88AYB867L5

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 sunmark triple antibiotic plus pain relief (source: ndc)
Generic Name polymyxin b sulfate, bacitracin zinc, neomycin 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
  • 36 TUBE in 1 CASE (50090-6172-0) / 28.4 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": "8ccae7c4-e443-4cec-a31d-764334293b65", "openfda": {"unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["01131ba6-6d5b-4710-bec3-ba1769c08c79"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "36 TUBE in 1 CASE (50090-6172-0)  / 28.4 g in 1 TUBE", "package_ndc": "50090-6172-0", "marketing_end_date": "20270831", "marketing_start_date": "20221014"}], "brand_name": "SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF", "product_id": "50090-6172_8ccae7c4-e443-4cec-a31d-764334293b65", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "50090-6172", "generic_name": "polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN 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_end_date": "20270831", "marketing_start_date": "20120331"}