GOODSENSE ANTIBACTERIAL MOISTURIZING- benzalkonium chloride film

GOODSENSE ANTIBACTERIAL MOISTURIZING by

Drug Labeling and Warnings

GOODSENSE ANTIBACTERIAL MOISTURIZING by is a Otc medication manufactured, distributed, or labeled by GEISS, DESTIN AND DUNN, INC., UNITED EXCHANGE CORP., AMERICAN HYGIENICS CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                                Purpose

Benzalkonium Chloride 0.115% ..........................................Antibacterial

PURPOSE

Uses

Decreases Bacteria on skin

WARNINGS

Warnings

For external use only.

WHEN USING

When using this product avoid contact with eyes.

If contact occurs, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash develops and persists for more than 72 hours.

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

• Pull top off lid by lifting upward.   Pull sheet from center of roll.  Insert corner of center sheet through flap opening on lid. Replace lid and pull sheet out at a 45 degree angle. The next sheet pops up automatically.  When finished, reseal by closing lid flap to retain moisture.   Do not push finger through dispenser hole.
• Apply thoroughly to hands and face as desired and allow to dry without wiping.
• Dispose of wipe in the proper container.
• Do not flush down the toilet
  

INACTIVE INGREDIENT

Inactive Ingredients

Purified Water, Alcohol, Propylene Glycol, Aloe Barbadensis Leaf Extract, Quatemium 52, PEG 60 Lanolin, Potassium Sorbate, Imidazolidinyl Urea Methyl Paraben, Propyl Paraben, Methylchloroisothiazolinone and Methylisothiazolinone, Disodium EDTA, Citric Acid, Fragrance

DOSAGE & ADMINISTRATION

Distributed By:

Geiss, Destin and Dunn, Inc.

Peachtree City, GA 30269

www.valuelabels.com

1-866-696-0957

Made in China

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

GOODSENSE ANTIBACTERIAL MOISTURIZING 
benzalkonium chloride film

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75981-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 g  in 100

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75981-004-59	40 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/21/2011

Labeler - GEISS, DESTIN AND DUNN, INC. (076059836)

Registrant - UNITED EXCHANGE CORP. (840130579)

Establishment
Name	Address	ID/FEI	Business Operations
AMERICAN HYGIENICS CORPORATION		545198454	manufacture