VITACILINA FIRST AID ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Taisho Pharmaceutical California Inc.

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Vitacilina First Aid Antibiotic

Drug Facts

Active ingredient (in each gram)

Bacitracin Zinc 400 units

Neomycin sulfate 3.5 mg

Polymyxin B sulfate 5,000 units

Purpose

First aid antibiotic

Use

First aid to help prevent infection in minor cuts, scrapes, and 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 to 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

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 15 to 30°C (59 to 86°F )
DO NOT USE IF SEAL ON TUBE IS BROKEN OR MISSING. Tamper Evident:

Inactive ingredient

petrolatum

Package Labeling 28g

Outer Package

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Inner Package

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Package Labeling 14g

Outer Package2 Inner Package2

VITACILINA FIRST AID ANTIBIOTIC
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:81929-003
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:81929-003-01	1 in 1 CARTON	07/01/2022
1		28 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC:81929-003-02	1 in 1 CARTON	07/01/2022
2		14 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M004	07/01/2022

Labeler - Taisho Pharmaceutical California Inc. (603827635)

Revised: 11/2023

Document Id: 09ce4763-a8f8-7cff-e063-6294a90a851c

Set id: 93fb9e05-f78c-4d37-b6f1-926cbcb2e7a7

Version: 2

Effective Time: 20231110

Taisho Pharmaceutical California Inc.