BACITRACIN- bacitracin ointment 
Cardinal Health

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Bacitracin Ointment

Active ingredient

Drug Facts :

Active ingredient (each gram contains) Bacitracin 500 units

Purpose

First aid antibiotic

Keep Out of Reach of Children

This package is intended for institutional use only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

First aid to help prevent infection in minor cuts, scrapes and 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, or serious burns Stop use and ask a doctor if you need to use longer than 1 week, condition persists or gets worse or a rash or other allergic reaction develops

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 and may be covered with a sterile bandage.

Inactive ingredients

Light mineral oil and white petrolatum

Storage

Store at 20 - 25 C (68 - 77 F)

Other

Manufactured for:

GOLDLINE LABORATORIES, INC.

a subsidiary of IVAX Pharmaceuticals, Inc.

Miami, FL 33137-3227

by: Perrigo Co.

Allegan, MI 49010

Questions? call 1-888-838-2872, weekdays 8 AM - 5 PM Eastern Time

Principal Display Panel

Bacitracin Ointment, USP

6 - 0.9 Gram Unit Dose Packets

bag label
BACITRACIN 
bacitracin ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-5844(NDC:0182-0208)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 
Inactive Ingredients
Ingredient NameStrength
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-5844-56 in 1 BAG06/02/201104/30/2012
11 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other06/02/201104/30/2012
Labeler - Cardinal Health (188557102)
Establishment
NameAddressID/FEIBusiness Operations
Cardinal Health188557102REPACK(55154-5844)

Revised: 1/2018
 
Cardinal Health