ALCOHOL- isopropyl alcohol swab

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Foodhold U.S.A. LLC, Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Uses

• For preparation of the skin prior to injection.
• First aid to decrease germs in minor cuts, scrapes and burns.
  

Warnings

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

Do not use

• with electrocautery procedures
• longer than 1 week unless directed by a doctor

When using this product

• do not get into eyes
• do not apply over large areas of the body
• in case of deep or puncture wounds, animal bites or serious burns, consult a doctor

Stop use and ask a doctor if

• irritation and redness develop
• condition gets worse or persists for more than 72 hours

Keep out of reach of children.

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

Directions

• Apply to skin as needed
• Discard after single use
  

Other information

Protect from freezing and avoid excessive heat.

Inactive Ingredients

Water

Principal Display Panel

NDC: 41520-809-30

CAREONE

Compare to the active ingredient in BD alcohol swabs

Individually foil wrapped

DO NOT USE IF PRODUCT IS TORN OR PUNCTURED

STERILE

Alcohol Prep Pads

70% Isopropyl Alcohol

• 2-ply pad offers excellent cleansing action
• Antiseptic for preparation of the skin prior to injection

100 swabs

Principal Display Panel

INGREDIENTS AND APPEARANCE

ALCOHOL 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41520-809
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: 41520-809-30	100 in 1 BOX
1		1 in 1 PACKET
1		0.5 mL in 1 APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2011

Labeler - American Sales Company, Inc. (809183973)