GOODSENSE ANTIBACTERIAL MOISTURIZING description, usages, side effects, indications, overdosage, supplying and lots more!

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GOODSENSE ANTIBACTERIAL MOISTURIZING

GEISS, DESTIN AND DUNN, INC.
UNITED EXCHANGE CORP.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                                                Purpose

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

Purpose

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.

Uses

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

GOODSENSE ANTIBACTERIAL MOISTURIZINGEnter section text here

GOODSENSE ANTIBACTERIAL MOISTURIZING

BENZALKONIUM CHLORIDE FILM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:75981-004
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.115 g

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
propylene glycol
Aloe Vera Leaf
POTASSIUM SORBATE
EDETATE DISODIUM
CITRIC ACID MONOHYDRATE

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
partA part333A 2011-02-21


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