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AMSure Alcohol Prep

Dosage form: swab
Ingredients: ISOPROPYL ALCOHOL 0.7mL in 1mL
Labeler: Amsino International, Inc.
NDC Code: 67752-0001

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.

Active Ingredient Section

Drug Facts

Active ingredient

Isopropyl Alcohol 70%

Purpose Section

Purpose

Antiseptic Cleanser

Keep Out Of Reach Of Children Section

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

Uses Section

Use For preparation of Skin prior to an injection.

Warnings Section

Warnings

  • For External Use Only
  • Flammable, Keep away from fire or flame
  • Do Not Use 1) with electrocautery procedures 2) In the eyes. If contact occurs, flush eyes with water
  • Stop Use If irritation and redness develop. If condition persists, contact your health care practitioner.
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions Section

Directions

Wipe injection site vigorously and discard

Other Information Section

Other information

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

Inactive Ingredient Section

Inactive ingredients

purified water

Package Label

NDC 67752-0001-1   AMSINO   AMSure Alcohol Prep Pad  Prep pad size 1-1/5"x1-1/5"   REF APP001S

STERILE   DO NOT REUSE   LATEX FREE

Distributed by: Amsino International, Inc.   855 Towne Center Dr., Pomona, CA 91767, USA

AMSure is a registered trademark of Amisino International, Inc.   L5666 Rev. A

TEAR HERE

AMSURE  ALCOHOL PREP
isopropyl alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67752-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:67752-0001-10.4 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2012
Labeler - Amsino International, Inc. (825673239)
Registrant - Amsino International, Inc. (825673239)

Revised: 03/2012
Document Id: 928c5bfc-70bc-4ff6-a6db-7b404538ec79
Set id: 5496aba5-f35b-46cc-bda9-5a89e30bb52a
Version: 2
Effective Time: 20120327
 
Amsino International, 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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