70%- isopropyl alcohol liquid

70% by

Drug Labeling and Warnings

70% by is a Otc medication manufactured, distributed, or labeled by Walgreens, CO., Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

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

for 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

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

For Rubbing or Massaging Caution

 Do not apply to irritated skin or if excessive irritation develops.  Avoid getting into the eyes or on mucous membranes.

Directions

• clean the affected area
• apply a small amount of this product on the affected 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

water

Adverse reactions

DISTRIBUTED  BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED  walgreens.com

810.003/810AA

principal display panel

Well at

Walgreens

NDC: 00363-0810-43

70%

Isopropyl

Alcohol

First Aid Antiseptic

For rubbing & massaging
WARNING

FLAMMABLE

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

USE ONLY IN A WELL-VENTILATED AREA; FUMES MAY BE HARMFUL

CAUTION: DO NOT POINT AT SEL OR OTHERS: PRODUCT WILL SQUIRT WHEN SQUEEZED.

16 FL OZ (1 PT) 473

INGREDIENTS AND APPEARANCE

70% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0810
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	500 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0810-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/15/1989
2	NDC: 0363-0810-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/15/1989
3	NDC: 0363-0810-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/15/1989

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/15/1989

Labeler - Walgreens, CO. (008965063)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(0363-0810)