HANDCLASP ISOPROPYL ALCOHOL ANTISEPTIC 75%- isopropyl alcohol solution

HANDCLASP ISOPROPYL ALCOHOL ANTISEPTIC 75% by

Drug Labeling and Warnings

HANDCLASP ISOPROPYL ALCOHOL ANTISEPTIC 75% by is a Otc medication manufactured, distributed, or labeled by BASF Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

• Active Ingredients(s): Purpose
• Isopropyl alcohol 75%v/v: Antiseptic

Use(s)

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

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

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

ASK DOCTOR

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

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)
  

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

INACTIVE INGREDIENT

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

PACKAGE LABEL

BASF
We create chemistry

HandClasp

Isopropyl Alcohol Antiseptic 75%
Topical Solution

Antiseptic Hand Rub
Non-sterile Solution

470 mL

BASF Corp. ● 1609 Biddle Avenue ● Wyandotte, MI ● 48192
1-800-526-1072

Batch: EX12345-1

Expiration Date: 9/27/2020

INGREDIENTS AND APPEARANCE

HANDCLASP ISOPROPYL ALCOHOL ANTISEPTIC 75% 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10117-1610
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302)	Isopropyl 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: 10117-1610-1	470 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
2	NDC: 10117-1610-2	940 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
3	NDC: 10117-1610-3	235 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2020
4	NDC: 10117-1610-4	5000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - BASF Corporation (014403088)

Establishment
Name	Address	ID/FEI	Business Operations
BASF Corporation		064197742	manufacture(10117-1610)