PUBLIX ALCOHOL- isopropyl alcohol swab

Publix Alcohol by

Drug Labeling and Warnings

Publix Alcohol by is a Otc medication manufactured, distributed, or labeled by Publix Super Markets, 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 an injection
• First aid to help 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

Package Label - Principal Display

Publix

NDC: 56062-826-30

Sterile

alcohol wipes

ANTISEPTIC

• for preparation of skin prior to injection
• Isopropyl Alcohol, 70% v/v
• convenient to use

100 INDIVIDUALLY SEALED WIPES

Package Label - Drug Facts & Side

INGREDIENTS AND APPEARANCE

PUBLIX ALCOHOL 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56062-826
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: 56062-826-30	100 in 1 BOX
1	NDC: 56062-826-09	1 in 1 PACKET
1		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	01/01/2013

Labeler - lix Super Markets Inc (006922009)