ISOPROPYL ALCOHOL solution

Isopropyl alcohol by

Drug Labeling and Warnings

Isopropyl alcohol by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 70%

Purpose

First aid antiseptic

Uses

first aid to help prevent the risk of infection in:

• minor cuts
• scrapes
• burns

Warnings

For external use only

Keep out of reach of children.

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

Caution

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

• 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

Other information

• does not contain, nor is intended as a substitute for grain or ethyl alcohol
• will produce serious gastric disturbances if taken internally

Inactive ingredients

blue 1, glycerin, methyl salicylate, water, yellow 5

SPL UNCLASSIFIED SECTION

REF MDS098003WZ

www.medline.com

Made in US with US and foreign components for Medline Industries, Inc.,

Mundelein, IL 60060 USA.

1-800-MEDLINE

PRINCIPAL DISPLAY PANEL

NDC: 53329-799-06

70% ISOPROPYL ALCOHOL

WITH GLYCERIN AND WINTERGREEN

First aid antiseptic

WARNING FLAMMABLE

Keep away from heat, spark, electrical fire or flame.

Product sealed for your protection.

Use only in a well-ventilated area; fumes can be harmful.

16 FL OZ

(1 PT) 473 mL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-799
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)
METHYL SALICYLATE (UNII: LAV5U5022Y)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-799-06	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/06/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/06/2015

Labeler - Medline Industries, Inc. (025460908)