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

Principal Display Panel - Box

Perincipal Display Panel Pouch

INGREDIENTS AND APPEARANCE

ALCOHOL PREP 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0012
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: 0924-0012-06	100 in 1 BOX	01/15/2016
1		0.55 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/15/2016

Labeler - Acme United Corporation (001180207)

Registrant - Dynarex Corporation (008124539)