SMITH AND JOHNSON ANTIBACTERIAL- triclosan soap

Smith and Johnson Antibacterial by

Drug Labeling and Warnings

Smith and Johnson Antibacterial by is a Otc medication manufactured, distributed, or labeled by Allied International Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Triclosan 0.115%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

USES: For hand washing to decrease bacteria on the skin.

WARNINGS

WARNING:

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Keep out of reach of children.

If swallowed, contact a poison control center immediately and consult a physician if necessary.

DOSAGE & ADMINISTRATION

DIRECTIONS

• Wet hands
• Apply palmful to hands
• Scrub thoroughly
• Rinse
  

WARNINGS AND PRECAUTIONS

WARNING: AS WITH ANY SOAP, AVOID CONTACT WITH EYES, IN CASE OF CONTACT, FLUSH WITH WATER.

DESCRIPTION

The Smith and  Johnson Liquid Soap is formulated to clean dirt and kill germs, an ideal high quality soap for the entire family.

INACTIVE INGREDIENT

INGREDIENTS: Water, Sodium Polyoxyethylene Fatty Alcohol Sulfate, Coconut Oil Diethanolamide, Citric Acid, Kathon CG, Fragrance, Sodium Chloride, FD and C Yellow No.5, FD and C Red No.40.

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ITEM Number: 20063 /  4492

MADE IN CHINA FOR

ALLIED INTERNATIONAL CORP.

Glen Burnie, MD 21060

www.alliedint.com

PRINCIPAL DISPLAY PANEL

Smith and Johnson

Liquid Soap

Antibacterial

16.9 FL.OZ (500ml)

INGREDIENTS AND APPEARANCE

SMITH AND JOHNSON ANTIBACTERIAL 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52546-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.115 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH-2 SULFATE (UNII: ZZQ59TY3KG)
COCONUT OIL (UNII: Q9L0O73W7L)
DIETHANOLAMINE (UNII: AZE05TDV2V)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 40 (UNII: WZB9127XOA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52546-110-00	500 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333E	05/19/2011

Labeler - Allied International Corp (004001780)