ALCOHOL PREP - isopropyl alcohol swab
Chain Drug Consortium, LLC

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.

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Alcohol Prep Pad

Active Ingredient Purpose

Isopropyl Alcohol 70% v/v Antiseptic

Use:alcohol prep

For preparation of the skin prior to injection.

Warnings:

For external use only
Flammable, keep away from flame or fire
Not for use with electrocautinary devices or procedures
Do not use in eyes

Indications and Usage:

Stop use and ask a doctor if:

Irritation or redness develops
condition persists for more than 72 hours
Cleansing of an injection site

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.

Directions:

Wipe injection site vigorously and discard

Other information:

Store at room temperature: 15 deg C to 30 deg C 59 deg F to 86 deg F
avoid excessive heat

Inactive Ingredient

Water

Principal Display Panel

alcohol_prep

ALCOHOL PREP
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:68016-012
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	1.4 mL

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

#	Item Code	Package Description
Packaging
1	NDC:68016-012-90	10 in 1 CASE
1		100 in 1 BOX

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/21/2011

Labeler - Chain Drug Consortium, LLC (101668460)