80% ALCOHOL HAND SANITIZER- alcohol solution 
Phoenix Products Company

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 rub manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Rub Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand rub 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 Rub

Use

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

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

Other information

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

KMS

* Effective at eliminating 99.9% of many

common harmful germs and bacteria.

** Meets the FDA healthcare personnel

antiseptic hand rub criteria

Made in USA

Empty &

Discard Pump

PLASTIC BOTTLE

how2recycle.info

Distributed by

KMS, Inc.

811 E Waterman St.

Wichita, KS 67208

SDA-NE-1013

0 79902 07899 8

ALCOHOL ANTISEPTIC 80 % TOPICAL SOLUTION

HAND
SANITIZER

KILLS 99.9% OF GERMS*

FORMULATED FOR HEALTHCARE**

GENTLE ENOUGH FOR EVERYDAY USE

NON-STERILE LIQUID SOLUTION

WARNING FOR EXTERNAL USE ONLY

FLAMMABLE. KEEP AWAY FROM HEAT OR FLAMES

64 FL OZ (1.89 L)

73956-301-64 Bottle Image

Package Label - Principal Display Panel

[Kinnos 8 oz]

kinnos

HAND SANITIZER

8 oz (237mL)

We started this company to
protect healthcare workers,
patients, and friends and
family from infections. At
Kinnos, our goal is to
empower people to protect
themselves and others, and
to provide society with
peace of mind.


Join us at www.kinnos.us


Alcohol Antiseptic
(80%)
Topical solution
Non-sterile

Manufactured by Kinnos Inc.

760 Parkside Avenue, Suite 219

Brooklyn, NY 11226

team@kinnos.us | (978) 314-3127

LB0009 Rev A

8 60949 00049 9

73956-401-08 Bottle Image

80% ALCOHOL HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73956-301
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) 18.42 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73956-301-641893 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
2NDC:73956-301-283785 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2020
80% ALCOHOL HAND SANITIZER 
alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73956-401
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) 18.42 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73956-401-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2020
Labeler - Phoenix Products Company (101332237)
Establishment
NameAddressID/FEIBusiness Operations
Phoenix Products Company101332237manufacture(73956-301, 73956-401)

Revised: 6/2020
Document Id: 1cf57abc-1491-417f-830b-303a85124120
Set id: a6cefe9f-6d3d-4ed0-87b7-bab9ca001d95
Version: 1
Effective Time: 20200601
 
Phoenix Products Company