SUNMARK  TRIPLE ANTIBIOTIC- polymyxin b sulfate, bacitracin zinc, and neomycin sulfate ointment 
McKesson

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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sunmark
triple antibiotic

Drug Facts

Active ingredients (in each gram)Purposes
Bacitracin 400 unitsFirst aid antibiotic
Neomycin 3.5 mg First aid antibiotic
Polymyxin B 5,000 unitsFirst aid antibiotic

Uses

first aid to help prevent infection in minor:

Warnings

For external use only

Do not use if you are allergic to any of the ingredients

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • do not use in the eyes
  • do not apply over large areas of the body

Stop use and ask a doctor if

  • you need to use for more than 1 week
  • condition persists or gets worse
  • symptoms persist for more than 1 week or clear up and occur again within a few days
  • 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

Other information

Inactive ingredient

white petrolatum

Distributed by McKesson
One Post Street
San Francisco, CA 94104

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

sunmark

triple antibiotic ointment

polymyxin B sulfate • bacitracin zinc • neomycin sulfate

First Aid Antibiotic

ORIGINAL STRENGTH

NET WT 1 OZ (28.4 g)

Principal Display Panel- 28.4 g Tube Carton
SUNMARK   TRIPLE ANTIBIOTIC
polymyxin b sulfate, bacitracin zinc, and neomycin sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-029
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
bacitracin zinc (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I) Bacitracin400 [iU]  in 1 g
neomycin sulfate (UNII: 057Y626693) (Neomycin - UNII:I16QD7X297) Neomycin3.5 mg  in 1 g
polymyxin B sulfate (UNII: 19371312D4) (Polymyxin B - UNII:J2VZ07J96K) Polymyxin B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
petrolatum (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-029-721 in 1 CARTON
128.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B12/14/1995
Labeler - McKesson (177667227)
Registrant - Taro Pharmaceuticals U.S.A., Inc. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295MANUFACTURE(49348-029)

Revised: 4/2013
Document Id: 45df6359-262f-442a-bdd5-c7d62d43a449
Set id: c07d4042-c5f0-4abc-8d5f-76893eec1fc8
Version: 2
Effective Time: 20130411
 
McKesson