AMSURE ALCOHOL PREP- isopropyl alcohol swab

AMSure by

Drug Labeling and Warnings

AMSure by is a Otc medication manufactured, distributed, or labeled by Amsino International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

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INGREDIENTS AND APPEARANCE

AMSURE  ALCOHOL PREP
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67752-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67752-0001-1	0.4 mL in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2012

Labeler - Amsino International, Inc. (825673239)

Registrant - Amsino International, Inc. (825673239)