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GOODSENSE ANTIBACTERIAL MOISTURIZING

Medically reviewed on Feb 21, 2018

Dosage form: film
Ingredients: BENZALKONIUM CHLORIDE 0.115g
Labeler: GEISS, DESTIN AND DUNN, INC.
NDC Code: 75981-004

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.

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

  • 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 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

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GOODSENSE ANTIBACTERIAL MOISTURIZING 
benzalkonium chloride film
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75981-004
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.115 g  in 100 
Inactive Ingredients
Ingredient NameStrength
WATER 
ALCOHOL 
PROPYLENE GLYCOL 
ALOE VERA LEAF 
POTASSIUM SORBATE 
EDETATE DISODIUM 
CITRIC ACID MONOHYDRATE 
Packaging
#Item CodePackage Description
1NDC:75981-004-5940 FILM (FILM) 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/FEIOperations
AMERICAN HYGIENICS CORPORATION545198454manufacture

 
GEISS, DESTIN AND DUNN, INC.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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