DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment

Drs. Pharmacy Triple Antibiotic Plus by

Drug Labeling and Warnings

Drs. Pharmacy Triple Antibiotic Plus by is a Otc medication manufactured, distributed, or labeled by OL PHARMA TECH, LLC Drs PHARMACY. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Bacitracin zinc 400 units
Neomycin 3.5 mg
Polymyxin B sulfate 5,000 units

Pramoxine hydrochloride 10 mg

Uses

first aid to help prevent infection in minor
cuts
scrapes
burns

Purpose

• first aid antibiotic
• External Analgesic

Do Not Use

Do not use
if you are allergic to any of the ingredients
in the eyes
over large areas of the body
longer than 1 week unless directed by a doctor

WARNINGS

For external use only

ASK DOCTOR

Ask a doctor before use if you have
deep or puncture wounds
animal bites
serious burns

STOP USE

Stop use and ask a doctor if
the condition persists or gets worse
a rash or other allergic reaction develops

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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 room temperature

Inactive Ingredient

Petrolatum

QUESTIONS

www.drspharmacyusa.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80489-757
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 1000 mg
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	3.5 mg  in 1000 mg
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [USP'U]  in 1000 mg
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg  in 1000 mg

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

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80489-757-01	1 in 1 CARTON	09/05/2021
1		14000 mg in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 80489-757-02	1 in 1 CARTON	09/05/2021
2		28300 mg 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	09/05/2021

Labeler - OL PHARMA TECH, LLC Drs PHARMACY (021170377)

Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)

Establishment
Name	Address	ID/FEI	Business Operations
OL PHARMA TECH, LLC Drs PHARMACY		021170377	manufacture(80489-757)