ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by UNFI, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Isopropyl alcohol 70%

Purpose

First aid antiseptic

Use

helps prevent the risk of infection in:

• minor cuts
• scrapes
• burns

Warnings

For external use only

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

Ask a doctor before use if

you have deep or puncture wounds, animal bites or serious burns

When using this product

• do not get into eyes
• do not inhale
• do not apply over large areas of the body
• do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

condition persists or gets worse

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 gettting 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 product serious gastric disturbances if taken internally

Inactive ingredients

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

SPL UNCLASSIFIED SECTION

Distributed by SUPERVALU INC.

Edne Prairie, MN 55344  USA

Contact us at 1-877-932-7948

or www.spervalue-ourbrands.com

845.003/845AE

principal display panel

NDC: 41163-845-43

EQUALINE

isopropyl rubbing alcohol

first aid antiseptic

wintergreen

70% isopropyl alcohol by volume

WARNING FLAMMABLE-Keep away from heat, spark, electrical, fire or flames

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

CAUTION: Do not point at self or others; product will squirt when squeezed

16 FL OZ (1PT) 473 mL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-845
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	613 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
METHYL SALICYLATE (UNII: LAV5U5022Y)
WATER (UNII: 059QF0KO0R)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41163-845-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/29/2005

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part344	07/29/2005

Labeler - Supervalu Inc (006961411)

Registrant - Vi-Jon Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		790752542	manufacture(41163-845)