ALCOHOL PREP- isopropyl alcohol swab

Alcohol Prep by

Drug Labeling and Warnings

Alcohol Prep by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation, Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                       Purpose

Isopropyl Alcohol 70% v/v                         Antiseptic

Purpose

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
• Sterile unless package is damaged or open.
  

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

Inactive Ingredient

• Water
  

Principal Display Panel - box

PRINCIPAL DISPLAY PANEL - 100 count box

PAK-KIT FIRST AID

STERILE ALCOHOL PREP PADS

Contains 100 single use alcohol prep pads.

See back panel for Drug Facts listing.

Distributed by: Acme United Corporation

Fairfield, CT 06824   800-835-2263

PK alcohol prep B.jpg

Principal Display Panel - packet

PRINCIPAL DISPLAY PANEL - packet

Dynarex Alcohol Prep Pad

STERILE ALCOHOL PREP PADS

Contains 1 single use alcohol prep pads.

Acme United Corporation 

Fairfield, CT 06824

PK alcohol prep P.jpg

INGREDIENTS AND APPEARANCE

ALCOHOL PREP 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0011
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: 0924-0011-06	100 in 1 BOX
1		0.55 mL in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/08/2014

Labeler - Acme United Corporation (001180207)

Registrant - Dynarex Corporation (008124539)