NEOMYCIN AND POLYMYXIN B SULFATES, AND BACITRACIN ZINC- neomycin sulfate, polymyxin b sulfate and bacitracin zinc ointment

Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc by

Drug Labeling and Warnings

Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc by is a Animal medication manufactured, distributed, or labeled by VetOne, Akorn, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

ANADA 200-553, Approved by FDA

DESCRIPTION:

Each gram contains: polymyxin B sulfate 10,000 units, bacitracin zinc 400 units, neomycin sulfate 5 mg (equivalent to 3.5 mg neomycin base) in a white petrolatum base, q.s.

ACTIONS:

Polymyxin B is one of a group of closely related substances produced by various strains of Bacillus polymyxa. The activity of polymyxin B is sharply restricted to gram-negative bacteria. Neomycin, isolated from Streptomyces fradiae, has antibacterial activity in vitro against a wide range of gram-negative and gram-positive organisms. Bacitracin, an antibiotic substance derived from cultures of Bacillus subtilis (Tracy), exerts antibacterial action in vitro against a variety of gram-positive and a few gram-negative organisms.

INDICATIONS:

This product is indicated for the treatment of superficial bacterial infections of the eyelid and conjunctiva of dogs and cats when due to organisms susceptible to one or more of the antibiotics contained in the ointment.

Laboratory tests should be conducted including in vitro culturing and susceptibility tests on samples collected prior to treatment.

PRECAUTIONS:

If irritation develops discontinue treatment with this drug. If there is no response to treatment in 2 to 3 days, discontinue treatment and re-evaluate diagnosis. Prolonged use may result in overgrowth of nonsusceptible organisms, including fungi.

Care should be taken not to contaminate the applicator tip during administration of the preparation.

ADVERSE REACTIONS:

Adverse reactions, such as itching, burning, or inflammation may occur in animals sensitive to this product.

DOSAGE AND ADMINISTRATION:

Properly cleanse area to be treated. Foreign bodies, crusted exudates and debris should be carefully removed. Express a small quantity of ointment into the conjunctival sac beneath the lower eyelid three or four times daily. After application hold the eyelids shut for a short time so that a thin film of ointment covers the cornea.

HOW SUPPLIED:

NDC: 13985-758-35 Tube of 3.5 g (1/8 oz) with ophthalmic tip.

STORAGE:

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temp].

KEEP OUT OF REACH OF CHILDREN.

Not for Human Use.

CAUTION: Federal (U.S.A.) law restricts this drug to use by or on the order of a licensed veterinarian.

Warning: Serious hypersensitivity (anaphylactic) reactions have been reported in cats within 4 hours of application of antibiotic ophthalmic preparations. Some of these reactions have resulted in death.

VET one®

Distributed by: MWI

Boise, ID 83705

www.VetOne.net

MWNB00n Rev. 03/18

PRINCIPAL DISPLAY PANEL

Principal Display Panel Text for Container Label:

Neomycin and Polymyxin B Sulfates, and

Bacitracin Zinc Ophthalmic Ointment, USP

For Veterinary Use Only ANADA 200-553, Approved by FDA

Sterile Ophthalmic Ointment Rx Only Net Weight: 3.5 g (1/8 oz)

PRINCIPAL DISPLAY PANEL

Principal Display Panel Text for Carton Label:

NDC: 13985-758-35 3.5 g

VET One® Logo

Neomycin and

Polymyxin B Sulfates,

and Bacitracin Zinc

Ophthalmic Ointment, USP

Sterile Ophthalmic Ointment

For Veterinary Use Only

Caution: Federal (U.S.A.) law

restricts this drug to use by or on the

order of licensed veterinarian.

Warning: Serious hypersensitivity

(anaphylactic) reactions have

been reported in cats within 4

hours of application of antibiotic

ophthalmic preparations. Some

of these reactions have resulted

in death.

ANADA 200-553. Approved by FDA

Rx only

V1 520010

Net Weight: 3.5 g (1/8 oz)

INGREDIENTS AND APPEARANCE

NEOMYCIN AND POLYMYXIN B SULFATES, AND BACITRACIN ZINC 
neomycin sulfate, polymyxin b sulfate and bacitracin zinc ointment

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 13985-758
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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	10000 [USP'U]  in 1 g
Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I)	Bacitracin	400 [USP'U]  in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 13985-758-35	1 in 1 CARTON
1		3.5 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANADA	ANADA200553	06/14/2018

Labeler - VetOne (019926120)

Registrant - Akorn, Inc. (062649876)

Establishment
Name	Address	ID/FEI	Business Operations
Akorn, Inc.		603980319	MANUFACTURE, ANALYSIS, STERILIZE, LABEL, PACK