LUCKY SUPERSOFT FIRST AID- bacitracin zinc ointment

Lucky SuperSoft by

Drug Labeling and Warnings

Lucky SuperSoft by is a Otc medication manufactured, distributed, or labeled by Delta Brands Inc, Anicare Pharmaceuticals Pvt. Ltd., Anicare Pharmaceuticals Pvt. ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each gram)

Bacitracin zinc 500 units

Purpose

First aid antibiotic

Uses

helps prevent infection in: ■ minor cuts ■ scrapes ■ burns

Warnings

For external use only

Alergy alert

■ do not use if allergic to any of the ingredients

Do not use

■ in eyes ■ on large areas of the body

Ask a doctor before use if you have

■ deep or puncture wounds ■ animal bites ■ serious burns

When using this product ■ do not use longer than 1 week

When using this product

■ do not use longer than 1 week

Stop use and ask a doctor if

■ condition lasts or 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 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 15-25C (59-77F) 

■ do not use if tube seal under cap is broken, missing or if the tube tip is cut prior to opening

Inactive ingredients

white petrolatum

Package Label

INGREDIENTS AND APPEARANCE

LUCKY SUPERSOFT  FIRST AID
bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 20276-104
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
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 20276-104-14	14 g in 1 PACKET; Type 0: Not a Combination Product	03/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	01/31/2015

Labeler - Delta Brands Inc (102672008)

Establishment
Name	Address	ID/FEI	Business Operations
anicare pharmaceuticals pvt ltd		916837425	manufacture(20276-104)