RUBBING ALCOHOL 50 PERCENT WITH WINTERGREEN- isopropyl alcohol liquid

RUBBING ALCOHOL by

Drug Labeling and Warnings

RUBBING ALCOHOL by is a Otc medication manufactured, distributed, or labeled by MY IMPORT USA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (BY VOLUME)

ISOPROPYL ALCOHOL (70% CONCENTRATE)

Purpose

FIRST AID ANTISEPTIC

Uses

FIRST AID TO HELP THE RISK OF INFECTION IN MINOR CUTS AND SCRAPES.

Keep Out of Reach of Children

IN CASE OF INGESTION, GET MEDICAL HELP OR CONTACT A POSON CONTROL CENTER (1-800-222-1222) IMMEDIATELY.

WARNINGS

For external use only.

• FLAMMABLE, KEEP AWAY FROM FIRE AND FLAME
• IF TAKEN NTERNALLY SERIOUS GASTRIC DISTURBANCES WILL RESULT

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

• STORE AT ROOM TEMPERATURE
• DOES NOT CONTAIN, NOR IS INTENDED AS A SUBSTITUTE FOR GRAIN OR ETHYL ALCOHOL

Inactive Ingredient

BLUE 1, METHYL SALICYLATE, WATER, YELLOW 5

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RUBBING ALCOHOL  50 PERCENT WITH WINTERGREEN
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-1014
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)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-1014-1	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/03/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/03/2014

Labeler - MY IMPORT USA INC (195767988)