80% Alcohol Hand Sanitizer

Manufacturer
Phoenix Products Company
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:18

Label at a glance#

Product80% Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

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.

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

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)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Rub

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

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 Image73956-301-64 Bottle Image

Package Label - Principal Display Panel

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 Image73956-401-08 Bottle Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73956-301-2880% Alcohol Hand Sanitizer3785 mL in 1 BOTTLESOLUTION37851
73956-301-6480% Alcohol Hand Sanitizer1893 mL in 1 BOTTLESOLUTION18931
73956-401-0880% Alcohol Hand Sanitizer237 mL in 1 BOTTLESOLUTION2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73956-30180% ALCOHOL HAND SANITIZER (ALCOHOL) SOLUTION [PHOENIX PRODUCTS COMPANY]1Legacy NDC, 2 package rows20200821_a6cefe9f-6d3d-4ed0-87b7-bab9ca001d95.zip
73956-40180% ALCOHOL HAND SANITIZER (ALCOHOL) SOLUTION [PHOENIX PRODUCTS COMPANY]1Legacy NDC, 1 package rows20200821_a6cefe9f-6d3d-4ed0-87b7-bab9ca001d95.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73956-30173956-301-64, 73956-301-28
73956-40173956-401-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1cf57abc-1491-417f-830b-303a85124120a6cefe9f-6d3d-4ed0-87b7-bab9ca001d952020-06-01WarningsExact identifier
spl id: 1cf57abc-1491-417f-830b-303a85124120
spl set id: a6cefe9f-6d3d-4ed0-87b7-bab9ca001d95

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.