Alcohol Wipes by Front Line Safety ALCOHOL WIPES swab

Alcohol Wipes by

Drug Labeling and Warnings

Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Front Line Safety. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Antiseptic

Use(s)

First aid to help prevent infection in minor cuts, scrapes, and burns.

For preparation of the skin prior to an injection.

Warnings

For External Use Only

Flammable. Keep away from fire or flame.

Do not use

In the eyes or over large areas of the body

Longer than 1 week unless directed by a doctor

With electrocautery procedures

Ask a doctor before use if you have

deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

condition persists for more than 72 hours or gets worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

When used for first aid: Clean the affected area. Apply a small amount of this product on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

When used to prepare an injection site: Apply product to the injection site prior to injection.

Other information

Store at room temperature 15º-30°C (59°-86ºF)

Avoid excessive heat

Inactive ingredients

Water

Questions?

1-888-900-2920 Monday-Friday, 8AM-4PM PST

PRINCIPAL DISPLAY PANEL

FL-2010

INGREDIENTS AND APPEARANCE

ALCOHOL WIPES 
alcohol wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58228-2610
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)

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58228-2610-1	1200 in 1 CASE	01/08/2024
1		50 in 1 BOX
1		0.55 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/08/2024

Labeler - Front Line Safety (061263699)