OPI topical solution hand sanitizer Non-sterile Solution Alcohol Antiseptic 80%

OPI topical solution hand sanitizer Non-sterile Solution Alcohol Antiseptic 80% by

Drug Labeling and Warnings

OPI topical solution hand sanitizer Non-sterile Solution Alcohol Antiseptic 80% by is a Otc medication manufactured, distributed, or labeled by Wella Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

OPI TOPICAL SOLUTION HAND SANITIZER NON-STERILE SOLUTION ALCOHOL ANTISEPTIC 80%- alcohol liquid 
Wella Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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OPI topical solution hand sanitizer Non-sterile Solution Alcohol Antiseptic 80%

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
2. Glycerol (1.45% v/v).
3. Hydrogen peroxide (0.125% v/v).
4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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.

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

Package Label - Principal Display Panel

110 mL NDC: 69282-010-01

OPI

topical solution

hand sanitizer

Non-sterile Solution

Alcohol Antiseptic 80%

For office use only.

Not for sale.

110 mL/ 3.75 fl. oz.

OPI TOPICAL SOLUTION HAND SANITIZER NON-STERILE SOLUTION ALCOHOL ANTISEPTIC 80% 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69282-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 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: 69282-010-01	110 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/24/2020	12/31/2021

Labeler - Wella Corporation (001399815)

Revised: 1/2022

Document Id: b67c3c45-0ed8-4375-e053-2a95a90aa910

34390-5

Set id: ad510795-d4a8-b9e9-e053-2a95a90ad100

Version: 2

Effective Time: 20220111