Hand Sanitizer Alcohol 80% Antiseptic

Hand Sanitizer Alcohol 80% by

Drug Labeling and Warnings

Hand Sanitizer Alcohol 80% by is a Otc medication manufactured, distributed, or labeled by Clarity Labs LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER ALCOHOL 80%- alcohol liquid 
Clarity Labs LLC

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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Hand Sanitizer Alcohol 80% Antiseptic

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

60 mL label FRONT & BACK60 mL NDC: 78232-001-01

240 mL NDC: 78232-001-02

500 mL NDC: 78232-001-03 240 mL label FRONT240 mL label BACK500 mL label FRONT  & BACK1 g or 3.7 L label FRONT & BACK

1 g NDC: 78232-001-04

HAND SANITIZER ALCOHOL 80% 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78232-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 1.45 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.125 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78232-001-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2020
2NDC: 78232-001-02240 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2020
3NDC: 78232-001-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2020
4NDC: 78232-001-043700 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/31/202006/23/2023
Labeler - Clarity Labs LLC (045246080)
Registrant - Clarity Labs LLC (045246080)
Establishment
NameAddressID/FEIBusiness Operations
Clarity Labs LLC045246080manufacture(78232-001)

Revised: 7/2021
 

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