GOODSENSE ANTIBACTERIAL MOISTURIZING - benzalkonium chloride film 
GEISS, DESTIN AND DUNN, INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient                                                                Purpose

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

Uses

Decreases Bacteria on skin

Warnings

For external use only.

When using this product avoid contact with eyes.

If contact occurs, rinse thoroughly with water.

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

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

Distributed By:

Geiss, Destin and Dunn, Inc.

Peachtree City, GA 30269

www.valuelabels.com

1-866-696-0957

Made in China

image of carton labelEnter section text here

GOODSENSE ANTIBACTERIAL MOISTURIZING 
benzalkonium chloride film
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75981-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.115 g  in 100 
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75981-004-5940 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/21/2011
Labeler - GEISS, DESTIN AND DUNN, INC. (076059836)
Registrant - UNITED EXCHANGE CORP. (840130579)
Establishment
NameAddressID/FEIBusiness Operations
AMERICAN HYGIENICS CORPORATION545198454manufacture

Revised: 2/2011
Document Id: be5e0db6-8ef6-43c8-9416-0af055f0c8ac
Set id: 2322576b-6f77-490c-a297-67a169e444d0
Version: 3
Effective Time: 20110221
 
GEISS, DESTIN AND DUNN, INC.