RUBBING ALCOHOL 99 PERCENT- isopropyl alcohol liquid

RUBBING ALCOHOL by

Drug Labeling and Warnings

RUBBING ALCOHOL by is a Otc medication manufactured, distributed, or labeled by Viny Health and Beauty Products Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ISOPROPYL ALCOHOL 99%

Purpose

FIRST AID ANTISEPTIC

Uses

FIRST AID TO HELP PREVENT THE RISK IN:

• MINOR CUTS
• SCRAPES
• BURNS

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

WARNINGS

For external use only.

FLAMMABLE

• KEEP AWAY FROM FIRE OR FLAME, HEAT, SPARK, ELECTRICAL.

FOR RUBBING AND MASSAGING: CAUTION - DO NOT APPLY TO IRRITATED SKIN OR IF EXCESSIVE IRRITATION DEVELOPS. AVOID GETTING INTO THE EYES OR ON MUCOUS MEMBRANES.

ASK DOCTOR

ASK A DOCTOR BEFORE USE IF YOU HAVE DEEP OR PUNCTURE WOUNDS, ANIMAL BITES OR SERIOUS BURNS

WHEN USING

WHEN USING THIS PRODUCT

• DO NOT GET INTO EYES
• DO NOT APPLY OVER LARGE AREAS OF THE BODY
• DO NOT USE LONGER THAN ONE WEEK UNLESS DIRECTED BY A DOCTOR

STOP USE

STOP USE AND ASK A DOCTOR IF CONDITION PERSISTS OR GET WORSE.

Directions

• CLEAN AFFECTED AREA
• APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 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 Ingredient

PURIFIED WATER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RUBBING ALCOHOL  99 PERCENT
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76436-306
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	99 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: 76436-306-16	475 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/07/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/07/2017

Labeler - Viny Health and Beauty Products Inc (963374942)