ALCOHOL EXTRA-THICK- isopropyl alcohol swab

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Meijer Distribution Inc, 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
• use only in a well ventilated area; fumes may be toxic

Stop use and ask a doctor if

• irritation and redness develop
• condition persists or gets worse or lasts 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

Package/Label Principal Display Panel

meijer

NDC: 41250-0040-82

compare to BD® Alcohol Swabs active ingredient*

Extra-Thick

Sterile

Alcohol Swabs

70% isopropyl alcohol, v/v

Antiseptic

For Preparation of the Skin Prior to Injection

Individually Wrapped Foil Packets

140 Pads

Package/Label Back

INGREDIENTS AND APPEARANCE

ALCOHOL  EXTRA-THICK
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41250-040
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: 41250-040-81	100 in 1 BOX
1		1 in 1 PACKET
1		5 mL in 1 APPLICATOR
2	NDC: 41250-040-82	140 in 1 BOX
2		1 in 1 PACKET
2		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	04/06/2011

Labeler - Meijer Distribution Inc (006959555)