HAND SANITIZER- alcohol liquid 
Elite Health Partners, 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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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

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

Other information

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

60 mL NDC: 74162-003-01 Hand Sanitizer 80 Percent Alcohol Antiseptic Topical Solution Non-Sterile 60 mL Flip-Top Bottle NDC 74162-003-01

60 mL NDC: 74162-003-02 Hand Sanitizer Alcohol Antiseptic 80 Percent Topical Solution Non-Sterile 60 mL Spray Bottle NDC 74162-003-02

60 mL NDC: 74162-003-03 NDC 74162-003-03 Hand Sanitizer Alcohol Antiseptic 80 Percent Topical Solution Non-Sterile

60 mL NDC: 74162-003-04 NDC: 74162-003-01 60 mL Hand Sanitizer Alcohol Antiseptic 80 Percent Topical Solution Non-Sterile

100 mL - UNLABELED - NOT FINAL PRODUCT - NDC:74162-003-06

60 mL - UNLABELED - NOT FINAL PRODUCT - NDC:74162-003-07

100 mL - Manufacturer NDC:74162-003-08, PLD NDC: 77429-001-01 100mL NDC 74162-003-08 Boulder Spirits Hand Sanitizing Rub 80% Alcohol Antiseptic Topical Solution Non-Sterile

60 mL - Manufacturer NDC:74162-003-05, PLD NDC:Waiting On FDA To Assign Labeler Code Undefined

60 mL - Manufacturer NDC:74162-003-09, PLD NDC: 78645-001-01 60 mL Hand Sanitizer 80% Alcohol Antiseptic SW Basics

HAND SANITIZER 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74162-003
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:74162-003-0160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/16/2020
2NDC:74162-003-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/08/2020
3NDC:74162-003-0360 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/24/2020
4NDC:74162-003-0460 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/09/2020
5NDC:74162-003-06100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2020
6NDC:74162-003-0760 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2020
7NDC:74162-003-08100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/17/2020
8NDC:74162-003-0560 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2020
9NDC:74162-003-0960 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/16/2020
Labeler - Elite Health Partners, LLC (081156583)
Establishment
NameAddressID/FEIBusiness Operations
Elite Health Partners, LLC081156583manufacture(74162-003)

Revised: 7/2020
Document Id: abbf5cd6-1be8-100a-e053-2a95a90a8b7a
Set id: a3fd49da-1f50-9d6c-e053-2a95a90a7054
Version: 10
Effective Time: 20200731
 
Elite Health Partners, LLC