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

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Active ingredients

Bacitracin zinc 500 units
Neomycin 3.5 mg
Polymyxin B sulfate 10,000 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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TRIPLE ANTIBIOTIC 2

DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-857
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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 B10000 [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:80489-857-011 in 1 CARTON09/05/2021
114000 mg in 1 TUBE; Type 0: Not a Combination Product
2NDC:80489-857-021 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 DrugM00309/05/2021
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(80489-857)

Revised: 4/2024
Document Id: 1626ff4b-c914-8681-e063-6294a90a1a2f
Set id: 1626fa89-cec0-6467-e063-6294a90aa2a4
Version: 1
Effective Time: 20240415
 
OL PHARMA TECH, LLC Drs PHARMACY