WISH RUBBING ALCOHOL 70% WINTERGREEN- isopropyl alcohol liquid

WISH RUBBING ALCOHOL 70% WINTERGREEN by

Drug Labeling and Warnings

WISH RUBBING ALCOHOL 70% WINTERGREEN by is a Otc medication manufactured, distributed, or labeled by LJ Pharma. 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 of infection 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 deepor 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 doctor

Stop use and ask doctor ifconditions persist or get worse

Keep out of reach of children In case of ingestion , get medical help or contact a poison. control center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

• Clean the 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 bandag.

Other information

• Store ate room temperature
• Does not contain, nor is intended as a substitute for grain or ethyl alchol.

Inactive Ingredients

Purified Water , Methyl Salicylate , FD&C GREEN #3, FD&C Yellow #5

Product label

INGREDIENTS AND APPEARANCE

WISH RUBBING ALCOHOL 70% WINTERGREEN 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84809-003
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 GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84809-003-01	12 in 1 CARTON	05/30/2025
1		355 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 84809-003-02	12 in 1 CARTON	05/30/2025
2		473 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 84809-003-03	12 in 1 CARTON	05/30/2025
3		946 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/30/2025

Labeler - LJ Pharma (914078633)

Establishment
Name	Address	ID/FEI	Business Operations
LJ Pharma		914078633	manufacture(84809-003)