ALCOHOL PAD- alcohol prep pad swab

Alcohol Pad by

Drug Labeling and Warnings

Alcohol Pad by is a Otc medication manufactured, distributed, or labeled by Redicare LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each towelette) ............Purpose

Isopropyl Alcohol 70%..........Antiseptic

Use:

For preparation of skin prior to injection.

Warnings:

• For external use only
• Flammable, keep away from fire or flame.

Do not use:

• With electrocautery procedures
• In the eyes

Stop use if

irritation and redness develop. If condition persists consult your health care practitioner.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison COntrol Center right away.

Directions:

Wipe injection area and discard.

Other information:

Store at room temperature 15 o to 30 oC (59 o to 86 oF).

Inactive ingredient:

water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOHOL PAD 
alcohol prep pad swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71105-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71105-111-03	50 in 1 BOX	03/31/2017
1	NDC: 71105-111-02	1 in 1 PACKET
1	NDC: 71105-111-01	0.45 g in 1 PATCH; 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	03/31/2017

Labeler - Redicare LLC (800149346)