EQUALINE  TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment 
Supervalu Inc

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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equaline™
triple antibiotic

Drug Facts

Active ingredient (each gram contains)Purpose
Bacitracin zinc 400 unitsFirst aid antibiotic
Neomycin sulfate 3.5 mgFirst aid antibiotic
Polymyxin B sulfate 5,000 unitsFirst aid antibiotic

Uses

first aid to help prevent infection in

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body
  • if you are allergic to any of the ingredients
  • longer than 1 week

Ask a doctor before use

  • on deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

  • 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

Other information

Inactive ingredients

white petrolatum

Distributed by
Albertsons, Inc.
Boise, Idaho 83726

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

equaline™

compare to Neosporin®
active ingredients*

first aid antibiotic
triple antibiotic ointment

polymyxin B sulfate • bacitracin zinc
neomycin sulfate

NET WT 0.5 OZ (14.2 g)

Principal Display Panel - 14.2 g Tube Carton
EQUALINE   TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-016
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:41163-016-011 in 1 CARTON
114.2 g in 1 TUBE
2NDC:41163-016-021 in 1 CARTON
228.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B12/14/1995
Labeler - Supervalu Inc (006961411)
Registrant - Taro Pharmaceuticals U.S.A., Inc. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295MANUFACTURE(41163-016)

Revised: 3/2013
Document Id: f8f88d9d-723a-4c5f-8000-b81745e994f5
Set id: 55ba9a6d-9dd9-433a-9221-c1075480e226
Version: 1
Effective Time: 20130306
 
Supervalu Inc