CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment

Curad Maximum Strength Triple Antibiotic by

Drug Labeling and Warnings

Curad Maximum Strength Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (in each gram)

Bacitracin 500 units

Neomycin 3.5 mg

Polymyxin B 10,000 units

Pramoxin hydrochloride 10 mg

Purposes

First aid antibiotic

First aid antibiotic

First aid antibiotic

Pain reliever

Uses

• First aid to help prevent infection in and temporarily relieves pain due to
• minor cuts
• scrapes
• burns

Warnings

• For external use only

Do not use

• if allergic to any of the ingredients
• in or near the eyes
• on 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 lasts or gets worse
• symptoms last for more than 7 days, or clear up and come back within a few days
• a rash or other allergic reaction develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 2 years and older:

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

Children under 2 years: ask a doctor

Other information

Store at controlled room temperature 68º-77ºF (20º-25ºC).

Inactive ingredient

petrolatum

SPL UNCLASSIFIED SECTION

©2019 CURAD and Medline are registered trademarks of Medline Industries, Inc. Manufactured for Medline Industries, Inc., Three Lakes Drive Northfield, IL 60093 USA. Made in USA of domestic and imported materials.
1-800-633-5463 RB19SFZ

Package Label

INGREDIENTS AND APPEARANCE

CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC 
bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	500 [USP'U]  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	10000 [USP'U]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-031-01	1 in 1 BOX	12/01/2019
1		28.4 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	12/01/2019

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Sheffield Pharmaceuticals LLC		151177797	manufacture(53329-031)