DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment 
OL PHARMA TECH, LLC Drs PHARMACY

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredients

Bacitracin zinc 400 units
Neomycin 3.5 mg
Polymyxin B sulfate 5,000 units

Pramoxine hydrochloride 10 mg

Uses

first aid to help prevent infection in minor
• cuts
• scrapes
• burns

Purpose

Do Not Use

Do not use
• if you are allergic to any of the ingredients
• in the eyes
• over large areas of the body
• longer than 1 week unless directed by a doctor

For external use only

Ask a doctor before use if you have
• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor if
• the condition persists or gets worse
• a rash or other allergic reaction develops

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• clean the affected area
• apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
• may be covered with a sterile bandage

OTHER INFORMATION

Store at room temperature

Inactive Ingredient

Petrolatum

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drs. Triple Antibiotic Plus

DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-757
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [USP'U]  in 1000 mg
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1000 mg
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1000 mg
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1000 mg
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80489-757-011 in 1 CARTON09/05/2021
114000 mg in 1 TUBE; Type 0: Not a Combination Product
2NDC:80489-757-021 in 1 CARTON09/05/2021
228300 mg in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B09/05/2021
Labeler - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
Establishment
NameAddressID/FEIBusiness Operations
OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-757)

Revised: 10/2023
Document Id: 06b99a44-3d0a-d5bf-e063-6394a90a5b41
Set id: d037bfb8-0d8c-4eda-e053-2995a90ae1f2
Version: 3
Effective Time: 20231002
 
OL PHARMA TECH, LLC Drs PHARMACY