ALCOHOL CLEANSING PAD- isopropyl alcohol liquid

Alcohol Cleansing Pad by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Active Ingredient:                                

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Use

 For preparation of skin before injection.

Warnings

 For external use only.  

STORAGE AND HANDLING

Flammable - keep away from fire or flame

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

DO NOT USE

Do not use: with electrocautery, in the eyes.

STOP USE

Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  If swallowed,

get medical help or contact a Poison Control

Center right away.

Directions

Wipe Injection site vigorously and discard.

Inactive Ingredient

Purified water.

SPL UNCLASSIFIED SECTION

LOT/EXP:            Made in CHINA

20140301

PRINCIPAL DISPLAY PANEL

Alcohol Cleansing Pad

Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

100 Alcohol cleansing pads

Reorder GFAP-39-02

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOHOL CLEANSING PAD 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52124-0002
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 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0002-1	0.5 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug	04/23/2010
2	NDC: 52124-0002-2	100 in 1 CARTON	04/23/2010
2		0.5 mL in 1 PACKAGE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
3	NDC: 52124-0002-3	10 in 1 BOX	04/23/2010
3		0.5 mL in 1 PACKET; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/23/2010

Labeler - Genuine First Aid LLC (619609857)