WALGREENS MAXIMUM STRENGTH TRIPLE ANTIBIOTIC WITH PAIN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hcl ointment 
Walgreen Co.

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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Walgreens Triple Antibiotic Pain Relieving Ointment 1 oz 910506 (2018)

Active ingredients (each gram contains)                                               Purpose

Bacitracin zinc 500 units.................................................................. First aid antibiotic

Neomycin sulfate 3.5 mg.................................................................. First aid antibiotic

Polymyxin B sulfate 10,000 units....................................................... First aid antibiotic

Pramoxine HCI 10 mg...................................................................... External analgesic

Uses

Warnings

For external use only

Do not use

Ask a doctor before use if you have

Stop use and ask a doctor if

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Other information

Inactive ingredients

ethanol, methylparaben, mineral oil, petrolatum, polyoxyl 40 stearate, propylparaben

Distributed by:

Walgreen Co.

200 Wilmot Rd.

Deerfield, IL 60015

Made in Korea

910506

WALGREENS MAXIMUM STRENGTH TRIPLE ANTIBIOTIC WITH PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hcl ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7872
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  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 B1000 [USP'U]  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
MINERAL OIL (UNII: T5L8T28FGP)  
PARAFFIN (UNII: I9O0E3H2ZE)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7872-281 in 1 CARTON05/13/2015
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B05/13/2015
Labeler - Walgreen Co. (008965063)

Revised: 3/2018
Document Id: 6664713c-8bd4-38c4-e053-2991aa0a7772
Set id: 1aef7104-94d9-436f-890b-d8371ba34aaf
Version: 3
Effective Time: 20180301
 
Walgreen Co.