TRIPLE ANTIBIOTIC CVS- bacitracin, neomycin, polymyxin ointment 
CVS

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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Drug Facts

Bacitracin 400 units, Neomycin 3.5 mg, Polymyxin B 5000 units

Uses

First aid to help prevent infection and for temporary relief of pain or discomfort in minor: cuts, scrapes, and burns.

Warnings

For external use only. Do not use in the eyes, over large areas of the body.  When using this product keep out of eyes.  Rinse eyes with water to remove.  Do not puncture or incinerate.  Contents under pressure. Ask a doctor before use if you have condition or symptoms get worse or last more than one week, symptoms clear up and occur again within a few days.

Directions

Adults and children 2 years of age and older:  clean the affected area, shake well before each use, spray a small amount of the product on the area 1 to 3 times daily.  May be covered with a sterile bandage.  Children under 2 years of age: consult a doctor.

Inactive ingredients

Glycerin, Hydrogenated Styrene/Butadiene Copolymer, Mineral Oil, Pentylene Glycol

Purpose

First aid antibiotic.


Keep out of reach of children.

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

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TRIPLE ANTIBIOTIC  CVS
bacitracin, neomycin, polymyxin ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-047
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B500 U  in 1 g
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 U  in 1 g
Inactive Ingredients
Ingredient NameStrength
Glycerin (UNII: PDC6A3C0OX)  
Mineral Oil (UNII: T5L8T28FGP)  
Pentylene Glycol (UNII: 50C1307PZG)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-047-0256 g in 1 CAN; Type 0: Not a Combination Product02/14/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B02/14/2014
Labeler - CVS (062312574)

Revised: 11/2017
Document Id: 43e6f421-b205-4159-9155-4ffa24b835f9
Set id: c1700671-5308-498d-92fc-e4a1ae9e1847
Version: 2
Effective Time: 20171120
 
CVS