WISH RUBBING ALCOHOL 91%- isopropyl alcohol liquid

WISH RUBBING ALCOHOL 91% by

Drug Labeling and Warnings

WISH RUBBING ALCOHOL 91% 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 91%

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, heat, sparks, electrical devices or use near open flame.
• Ask a doctor before useif 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 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.

Caution: Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or excessive amounts. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

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

Product label

INGREDIENTS AND APPEARANCE

WISH RUBBING ALCOHOL 91% 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84809-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	91 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: 84809-011-01	12 in 1 CARTON	01/20/2026
1		473 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 84809-011-02	8 in 1 CARTON	01/20/2026
2		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	01/20/2026

Labeler - LJ Pharma (914078633)

Establishment
Name	Address	ID/FEI	Business Operations
LJ Pharma		914078633	manufacture(84809-011)