FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF- neomycin sulfate ointment

FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF by

Drug Labeling and Warnings

FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by UNITED EXCHANGE CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients (each gram contains)                                                    Purpose

Neomycin Sulfate 3.5 mg.........................................................................Antibiotic

PURPOSE

Uses

first aid to help prevent infection in

• minor cuts
• scrapes
• burns

WARNINGS

Warnings

For external use only

DO NOT 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 DOCTOR

Ask a doctor before use in case of deep or puncture wounds, animal bites, or 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

INDICATIONS & USAGE

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
  

STORAGE AND HANDLING

Other information

• store at 15o to 25oC (59o to 77oF)
• Lot No. and Exp. Date: see box or see crimp of tube
  

INACTIVE INGREDIENT

Inactive ingredients

liquid paraffin, cetanol, squalane, white petrolatum, stearyl alcohol, tocopherol acetate, purified lanolin, methyl parahydroxybenzoate, propyl parahydroxybenzoate

DOSAGE & ADMINISTRATION

Distributed by:

UNITED EXCHANGE CORP.

17211 Valley View Ave.

Cerritos, CA 90703 USA

Made in Korea

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

FAMILY CARE TRIPLE ANTIBIOTIC PAIN RELIEF 
neomycin sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
SQUALANE (UNII: GW89575KF9)
PETROLATUM (UNII: 4T6H12BN9U)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
LANOLIN (UNII: 7EV65EAW6H)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-007-23	1 in 1 CARTON
1		28 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	02/07/2012

Labeler - UNITED EXCHANGE CORP. (840130579)