DABUR FIRST AID- bacitracin zinc ointment

dabur by

Drug Labeling and Warnings

dabur by is a Otc medication manufactured, distributed, or labeled by Dabur India Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each gram)

Bacitracin Zinc (equal to 500 bacitracin units)

Purpose

First Aid Antibiotic

Uses

■ first aid to help prevent infection in minor ■ cuts ■ scrapes ■ burns

Warnings

For external use only

Do not use

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

Ask a doctor before use in case of

■ deep or puncture wounds

■ animal bites ■ serious burns

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.

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 15-30C (59-86F)

■ avoid excessive heat and humidity

Inactive Ingredients

hard paraffin, liquid paraffin, white soft paraffin, lanolin

Package Label

INGREDIENTS AND APPEARANCE

DABUR  FIRST AID
bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68747-3035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 [USP'U]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN (UNII: 7EV65EAW6H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68747-3035-2	0.9 g in 1 PACKET; Type 0: Not a Combination Product	05/30/2013
2	NDC: 68747-3035-3	14 g in 1 TUBE; Type 0: Not a Combination Product	05/30/2013
3	NDC: 68747-3035-4	28 g in 1 TUBE; Type 0: Not a Combination Product	05/30/2013
4	NDC: 68747-3035-5	113 g in 1 TUBE; Type 0: Not a Combination Product	05/30/2013
5	NDC: 68747-3035-6	425 g in 1 JAR; Type 0: Not a Combination Product	05/30/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	05/30/2013

Labeler - Dabur India Limited (650319218)