CVS HEALTH ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol aerosol, spray

CVS Health Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

CVS Health Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 70% by volume

Purpose

First aid antiseptic

Uses

• first aid to help prevent the risk of infection in minor cuts, scrapes and burns
• helps relieve minor muscular aches due to exertion

Warnings

For external use only. Flammable,keep away from heat, spark, electrical, fire or flame 

• will produce serious gastric disturbances if taken internally

Do not use

• in the eyes or apply over large areas of the body 
• longer than 1 week 
• do not inhale

Ask a doctor before use if you have

deep or puncture wounds, animal bites or serious burns.

Stop use and ask a doctor if

• the condition persists or gets worse 
• irritation, pain, or redness persists or worsens 
• swelling, rash, or fever develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• clean the affected area 
• apply a small amount of product on the affected area 1 to 3 times a day 
• may be covered with a sterile bandage 
• if bandaged, let dry first

Other information

• keep tightly closed and at controlled room temperature 
• does not contain, nor is it intended as a substitute for grain or ethyl alcohol

Inactive ingredients

Nitrogen, Purified Water, Sodium Benzoate

Package Labeling:

INGREDIENTS AND APPEARANCE

CVS HEALTH ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-979
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 g

Inactive Ingredients
Ingredient Name	Strength
NITROGEN (UNII: N762921K75)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-979-00	85 g in 1 CONTAINER; Type 0: Not a Combination Product	03/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/19/2024

Labeler - CVS Pharmacy, Inc (062312574)