Gobrands, Inc. Triple Antibiotic Ointment Drug Facts

goodnow triple antibiotic by

Drug Labeling and Warnings

goodnow triple antibiotic by is a Otc medication manufactured, distributed, or labeled by Gobrands, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GOODNOW TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin, polymyxin b ointment 
Gobrands, Inc

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Gobrands, Inc. Triple Antibiotic Ointment Drug Facts

Active ingredients (in each gram)

Bacitracin zinc equivalent to 400 units bacitracin

Neomycin sulfate equivalent to 3.5 mg of neomycin base

Polymyxin B 5,000 units as polymyxin B sulfate

Purpose

First aid antibiotic

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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

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

cocoa butter, cottonseed oil, olive oil, sodium pyruvate, tocopheryl acetate, white petrolatum

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to active ingredients in Neosporin®

good™ now

ORIGINAL STRENGTH

Triple Antibiotic Ointment

Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate

NET WT 1 OZ (28 g)

First Aid Antibiotic

24-Hour Infection Protection

GOODNOW TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin, polymyxin b ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82501-0067
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
COCOA BUTTER (UNII: 512OYT1CRR)
COTTONSEED OIL (UNII: H3E878020N)
OLIVE OIL (UNII: 6UYK2W1W1E)
SODIUM PYRUVATE (UNII: POD38AIF08)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Product Characteristics
Color	WHITE (Translucent)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82501-0067-0	1 in 1 CARTON	04/12/2023	04/30/2025
1		28 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 Drug	M004	04/12/2023	04/30/2025

Labeler - Gobrands, Inc (057499049)

Revised: 6/2025

Document Id: 041abf6a-3985-4559-be3f-a0ab8507758c

34390-5

Set id: ad9763d7-2f23-43a5-9bdb-2068a9254bbb

Version: 4

Effective Time: 20250604