UP AND UP BACITRACIN FIRST AID- bacitracin ointment
Target 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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Target Corporation Bacitracin Drug Facts

Active ingredient (each gram contains)

Bacitracin 500 units

Purpose

First aid antibiotic

Uses

first aid to help prevent infection in:

•: minor cuts
•: scrapes
•: burns

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

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

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 this 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

Other information

•: store at 20°-25°C (68°-77°F)

Inactive ingredients

light mineral oil, white petrolatum

Questions?

Call 1-800-910-6874

Principal Display Panel

bacitracin

first aid antibiotic ointment

helps prevent infection in minor cuts, scrapes and burns

Bacitracin Carton Image 1

Bacitracin Carton Image 2

UP AND UP BACITRACIN FIRST AID
bacitracin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-536
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 [USP'U] in 1 g

Ingredient Name	Strength
Inactive Ingredients
LIGHT MINERAL OIL (UNII: N6K5787QVP)
PETROLATUM (UNII: 4T6H12BN9U)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11673-536-64	1 in 1 CARTON	11/29/2009	12/01/2016
1		28 g in 1 TUBE; 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	11/29/2009	12/01/2016

Labeler - Target Corporation (006961700)

Revised: 11/2017

Document Id: 418fc06d-81e1-43ef-98ec-176b25d98c76

Set id: e7b2b409-9385-418f-9480-627507fdfa0f

Version: 3

Effective Time: 20171105

Target Corporation