MED PRIDE 70% ISOPROPYL RUBBING ALCOHOL

Drug Labeling and Warnings

Drug Details [pdf]

RUBBING ALCOHOL 70 PERCENT- isopropyl alcohol liquid 
Viny Health and Beauty Products Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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MED PRIDE 70% ISOPROPYL RUBBING ALCOHOL

Active ingredient

ISOPROPYL ALCOHOL, 70%

Purpose

FIRST AID ANTISEPTIC

Uses

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

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 AND FLAMEEAT, SPARK, ELECTRICITY
• IF TAKEN NTERNALLY, SERIOUS GASTRIC DISTURBANCES WILL RESULT

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 ONE WEEK UNLESS DIRECTED BY A DOCTOR
• DO NOT USE OTHERWISE THAN DIRECTED

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

Directions

• CLEAN THE AFFECTED AREA
• APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 TIMES DAILY
• IF BANDAGED, LET DRY FIRST
• MAY BE COVERED WITH A STERILE BANDAGE

OTHER INFORMATION

• STORE AT ROOM TEMPERATURE
• 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

RUBBING ALCOHOL  70 PERCENT
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76436-308
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76436-308-16	475 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2017
2	NDC: 76436-308-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/30/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/30/2017	07/21/2019

Labeler - Viny Health and Beauty Products Inc (963374942)

Revised: 7/2019

Document Id: 7a8cdd04-1ff8-4afc-97b4-301e13a689ad

34390-5

Set id: 39789b21-bbdc-4f04-83ee-8ad672de4347

Version: 5

Effective Time: 20190721