ISOPROPYL ALCOHOL- isopropyl alcohol spray spray

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 70%

Purpose

First Aid Antiseptic

Use(s)

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For External Use Only

Do not use

Near eyes or mucous membranes Over large areas of the body Longer than 1 week unless directed by a doctor With electrocautery procedures

Ask a doctor before use if you have

Deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

Condition persists for more than 72 hours or get worse.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Clean the affected area and spray 1 to 3 times daily May be covered with a sterile bandage If bandaged, let dry first

Children under 12 years of age: Consult a doctor before use

Other Information

Store at 20º-25ºC

Avoid excessive heat

Inactive Ingredient

Purified Water

Questions?

1-888-Dynarex Monday - Friday, 9AM - 5PM EST

Label 1166

Isopropyl Alcohol Spray

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-011-01	24 in 1 CASE	02/29/2024
1	NDC: 67777-011-02	59.1 mL in 1 BOTTLE, SPRAY; 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	02/29/2024

Labeler - Dynarex Corporation (008124539)