HAND SANITIZER- ethyl alcohol liquid

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Everbrands, Inc. dba EverPure, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients

Alcohol 80%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses Hand sanitizer to help reduce bacteria
that potentially can cause disease. For use
when soap & water are not available.

WARNINGS

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

DO NOT USE

Do not use
in children less than 2 months of age
on open skin wounds

WHEN USING

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

STOP USE

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

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

OTHER SAFETY INFORMATION

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

DOSAGE & ADMINISTRATION

Directions Place enough product on hands to
cover all surfaces. Rub hands together until dry

INACTIVE INGREDIENT

Inactive ingredients glycerin, hydrogen
peroxide, purifed water USP

Product Label

H&​™  by EverPure​™

unscented

Hand

Sanitizer

99.9% effective

against most germs

antiseptic

4 FL. OZ.

visit everpurecare.com for more information

EverPure, Inc.
401 N. Oak St.
Inglewood, CA
90302

8 51036 00888 7

1 OZ

2 OZ

4OZ

res

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72655-021
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: 72655-021-04	29.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/09/2020
2	NDC: 72655-021-05	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/09/2020
3	NDC: 72655-021-06	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/09/2020

Labeler - Everbrands, Inc. dba EverPure, Inc. (080314845)

Registrant - Everbrands, Inc. dba EverPure, Inc. (080314845)

Establishment
Name	Address	ID/FEI	Business Operations
Everbrands, Inc. dba EverPure, Inc.		080314845	manufacture(72655-021)