ISOPROPYL ALCOHOL ANTISEPTIC- alcohol solution

Isopropyl Alcohol Antiseptic by

Drug Labeling and Warnings

Isopropyl Alcohol Antiseptic by is a Otc medication manufactured, distributed, or labeled by Hill Dermaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient[s}

Isopropyl alcohol 75% v/v

Purpose

Antiseptic

Use[s]

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Question?

1-800-344-5707

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

HILL DERM
PHARMACY, INC.™

Isopropyl Alcohol
Antiseptic 75%
Topical Solution

Hand Sanitizer
Non-sterile Solution

100 mL

MADE IN A
FDA
REGISTERED
FACILITY

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL ANTISEPTIC 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 28105-705
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
glycerin (UNII: PDC6A3C0OX)
hydrogen peroxide (UNII: BBX060AN9V)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 28105-705-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	04/01/2020

Labeler - Hill Dermaceuticals, Inc. (098366990)

Establishment
Name	Address	ID/FEI	Business Operations
Hill Dermaceuticals, Inc.		098366990	MANUFACTURE(28105-705)