ISOPROPYL RUBBING ALCOHOL 99 PERCENT- isopropyl alcohol solution

ISOPROPYL RUBBING ALCOHOL by

Drug Labeling and Warnings

ISOPROPYL RUBBING ALCOHOL by is a Otc medication manufactured, distributed, or labeled by MY Sales LLC dba Click Products LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

ISOPROPYL ALCOHOL (99% CONC.)

Purpose

FIRST AID ANTISEPTIC

Uses

FIRST AID TO HELP PREVENT THE RISK IN:

• MINOR CUTS
• SCRAPES
• BURNS

WARNINGS

FOR EXTERNAL USE ONLY.

• IF TAKEN INTERNALLY, SERIOUS GASTRIC DISTURBANCES WILL RESULT.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME

• USE ONLY IN A WELL-VENTILATED AREA; FUMES MAY BE TOXIC.

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

WHEN USING THIS PRODUCT

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

STOP USE AND ASK A DOCTOR IF CONDITIONS PERSIST OR GET WORSE.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. IN CASE OF INGESTION, GET MEDICAL HELP OR CONTACT A POSON CONTROL CENTER RIGHT AWAY.

Directions

• CLEAN AFFECTED AREA
• APPLY SMALL AMOUNT OF THIS PRODUCT ON THE AREA 1-3 TIMES DAILY
• LET THE ALCOHOL DRY ON SKIN BEFORE USING BANDAGES
• 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

Inactive Ingredient

PURIFIED WATER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ISOPROPYL RUBBING ALCOHOL  99 PERCENT
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71611-402
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: 71611-402-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/25/2020
2	NDC: 71611-402-01	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/25/2020

Labeler - MY Sales LLC dba Click Products LLC (080766174)