WHITE DOVE 70 PERCENT ALCOHOL ISOPROPYL- isopropyl alcohol solution

WHITE DOVE 70 PERCENT ALCOHOL ISOPROPYL by

Drug Labeling and Warnings

WHITE DOVE 70 PERCENT ALCOHOL ISOPROPYL 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 70%

Purpose

FIRST AID ANTISEPTIC

Uses

FIRST AID TO HELP PREVENT THE RISK IN:

• MINOR CUTS
• SCRAPES BURNS

Keep Out of Reach of Children

IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

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.

WARNINGS

For external use only.

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

ASK DOCTOR

ASK A DOCTOR BEFORE USE IF YOU HAVE

• DEEP PUNCTURE WOUNDS 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 1 WEEK UNLESS DIRECTED BY A DOCTOR.

STOP USE

STOP USE AND ASK A DOCTOR IF

• CONDITION PERSISTS OR GET WORSE.

Directions

• CLEAN THE AFFECTED AREA.
• APPLY A SMALL AMOUNT OF THIS PRODUCT ON THE 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 Ingredient

WATER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHITE DOVE 70 PERCENT ALCOHOL ISOPROPYL 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76436-320
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: 76436-320-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/24/2024

Labeler - Viny Health and Beauty Products Inc (079977276)