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GOODSENSE Alcohol

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 70g in 100g
Labeler: GEISS, DESTIN AND DUNN, INC.
NDC Code: 75981-001

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.

GOODSENSE Alcohol Swabs

Drug Facts

Active Ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Use For preparation of the skin prior to an injection

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not use

  • with electrocautery procedures
  • in the eyes.

Stop use if irritation or redness develop. If the condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or Contact a Poison Control Center right away.

Directions

Wipe injection site vigorously and discard

Other Information
Store at room temperature: 15 degrees - 30 degrees C (59 degrees - 86 degrees F)

Inactive ingredient

purified water

* This product is not manufactured or distributed by Becton, Dickinson and Company, owner of the registered trademark, BD.

Distributed by:
Geiss, Destin and Dunn Inc.
Peachtree City, GA 30269
www.valuelabels.com
1-866-696-0957
Made In China

GOODSENSE

70% Isopropyl Alcohol

Alcohol Swabs
Sterile
  • Antiseptic for preparation of the skin prior to injection
  • Convenient to use
100 Individual Pads

Compare to active ingredient of
BD Alcohol Swabs
100% SATISFACTION GUARANTEED





GOODSENSE ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75981-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL70 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:75981-001-00100 PACKET (SWAB) in 1 BOX
10.5 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/30/2011
Labeler - GEISS, DESTIN AND DUNN, INC. (076059836)
Registrant - Planet (Suzhou) Medical Products Co., Ltd (528194366)
Establishment
NameAddressID/FEIOperations
Planet (Suzhou) Medical Products Co., Ltd528194366manufacture

Revised: 06/2011
Document Id: 64004b37-45f5-4c5d-a712-929413eff18b
Set id: af18180a-b94d-41e1-90aa-b8bd42c10630
Version: 1
Effective Time: 20110630
 
GEISS, DESTIN AND DUNN, INC.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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