70%- isopropyl alcohol liquid

70% by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Isopropyl alcohol

Purpose

First Aid Antiseptic

Use

First aid to help 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 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 hep or contact a Poison Control Center right away

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 Perrigo

Minneapolis, MN 55427

810.003/810AA

principal display panel

Perrigo

NDC: 0574-0067-16

Isopropyl

Rubbing

Alcohol

70% USP

First Aid Antiseptic

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 self or others; product will squirt when squeezed

16 FL OZ

(1 PT) 473 mL

INGREDIENTS AND APPEARANCE

70% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0574-0067
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: 0574-0067-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/14/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/14/2014

Labeler - Paddock Laboratories LLC (967694121)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(0574-0067)