BACITRACIN ZINC, NEOMYCIN SULFATE AND POLYMYXIN B SULFATE - bacitracin zinc, neomycin sulfate and polymyxin b sulfate ointment 
Dynarex Corporation

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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Triple Antibiotic

Active ingredient (in ea. gram)                                                Purpose           
Bacitracin Zinc 400 Units                                                                      antibacterial

Neomyxin Sulfate 5mg (Equivalent to 3.5 mg Neomyxin)                         antibacterial

Polymyxin B Sulfate 5000 Units                                                            antibacterial

Uses triple antibiotic :

First aid to help prevent infection in:

Ask a doctor before use:


Other information

Inactive ingredients:

White petrolatum

Directions triple antibiotic:

KEEP OUT OF REACH OF CHILDREN  If swallowed, get medical help or contact a Poison Control Center right away.

First aid antibacterial ointment to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only

Principal Display Panel

Triple Antibiotic

triple_antibiotic

BACITRACIN ZINC, NEOMYCIN SULFATE AND POLYMYXIN B SULFATE 
bacitracin zinc, neomycin sulfate and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-240
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN ZINC - UNII:89Y4M234ES) BACITRACIN ZINC400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-240-0112 in 1 CASE
1144 in 1 BOX
10.5 g in 1 PACKET
2NDC:67777-240-0212 in 1 CASE
2144 in 1 BOX
20.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B03/16/2011
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 3/2011
Document Id: 17776a1c-d279-4cdc-8860-ce18c2ceca34
Set id: 650d1b78-005c-41eb-9df4-67a5d576c02b
Version: 3
Effective Time: 20110323
 
Dynarex Corporation