WALGREENSTRIPLE ANTIBIOTIC- bacitracin, neomycin, polymyxin b ointment
Walgreen Company

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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Package Labeling

Drug Facts

Active Ingredients (in each gram)

Bacitracin 400 units

Neomycin 3.5 mg

Polymyxin B 5,000 units

Uses

first aid to help prevent infection in minor:
• cuts • scrapes • burns

Warnings

For external use only.

Do not use

• if you are allergic to any of the ingredients

• in the eyes

• over large areas of the body

Ask a doctor before use if you have

• deep or puncture wounds • animal bites • serious burns

Stop use and ask a doctor if

• you need to use longer than 1 week

• condition persists or gets worse

• rash or other allergic reaction develops • side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

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

Directions

• clean the affected area • apply a small amount of product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily • may be covered with a sterile bandage

Inactive Ingredients

white petrolatum

Purpose

First Aid Antibiotic

Other information

•store at 15° to 25°C (59° to 77°F) • prior to initial use, please prime pump by
depressing multiple times

Questions or Comments?

1-800-635-3696

card label

WALGREENSTRIPLE ANTIBIOTIC
bacitracin, neomycin, polymyxin b ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-7123
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [USP'U] in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [USP'U] in 1 g

Ingredient Name	Strength
Inactive Ingredients
PETROLATUM (UNII: 4T6H12BN9U)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-7123-01	1 in 1 PACKAGE	07/01/2008	10/24/2016
1		7.7 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333B	07/01/2008	10/24/2016

Labeler - Walgreen Company (008965063)

Registrant - Wisconsin Pharmacal Company (800873986)

Name	Address	ID/FEI	Business Operations
Establishment
Wisconsin Pharmacal Company		800873986	manufacture(0363-7123)

Revised: 12/2017

Document Id: 5f8ad9e0-ddbc-1c24-e053-2a91aa0ad070

Set id: f32137d3-9616-4528-a3e2-62a1436511ca

Version: 5

Effective Time: 20171204

Walgreen Company