THERA PLUS ORIGINAL STRENGTH TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment

Thera Plus Original Strength Triple Antibiotic by

Drug Labeling and Warnings

Thera Plus Original Strength Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by FOURSTAR GROUP USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Bacitracin zinc 400 units

Neomycin sulfate 3.5 mg

Polymyxin B sulfate 5,000 units

Purpose

First aid antibiotic

Uses

for first aid to help to 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 this product
• in contact with the eyes or mucous membranes
• over large areas of the body
• longer than 1 week unless directed by a doctor

When using this product

• avoid contact with eyes

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor if

• symptoms last for more than 7 days
• the condition persists or gets worse
• symptoms clear up and then occur again within a few days
• a rash or other allergic reaction occurs

Keep out of reach of children.

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

Directions

Adults and children 2 years of age and older:

• clean the affected area
• apply a small amount of this product (an amount equal to the surface area of the tip of a finger) to affected area 1 to 3 times daily
• May be covered with a sterile bandage.
• Children under 2 years of age: ask a doctor before use

Other information

• store at room temperature 59° - 77°F (15° - 25°C).

Inactive ingredients

mineral oil, petrolatum

Questions?

1-800-639-3803Weekdays 9 AM to 4 PM EST

Package Labeling:

INGREDIENTS AND APPEARANCE

THERA PLUS ORIGINAL STRENGTH TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80684-140
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 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 U  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80684-140-00	14 g in 1 TUBE; Type 0: Not a Combination Product	03/03/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	03/03/2025

Labeler - FOURSTAR GROUP USA, INC. (140099503)