FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Everbrands, Inc. dba EverPure, Inc.
Effective date
2020-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:36

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Alcohol 80%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

Do not use
• 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.

OTHER SAFETY INFORMATION

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

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, hydrogen
peroxide, purifed water USP

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

021-04 1oz021-04 1oz

2 OZ

021-05 2oz021-05 2oz

4OZ

021-06 4oz021-06 4oz

res

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72655-021-042023-01-30C16284748780-1f386c64a-45ab-0266-e053-dadaa90a7c1aHand Sanitizer
72655-021-052023-01-30C16284748780-1f386c64a-45ab-0266-e053-dadaa90a7c1aHand Sanitizer
72655-021-062023-01-30C16284748780-1f386c64a-45ab-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72655-021-04Hand Sanitizer29.5 mL in 1 BOTTLE, PLASTICLIQUID29.51
72655-021-05Hand Sanitizer59 mL in 1 BOTTLE, PLASTICLIQUID591
72655-021-06Hand Sanitizer118 mL in 1 BOTTLE, PLASTICLIQUID1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72655-021HAND SANITIZER (ETHYL ALCOHOL) LIQUID [EVERBRANDS, INC. DBA EVERPURE, INC.]1Legacy NDC, 3 package rows20200410_4538f141-8055-4262-99d7-fe2cd9cc7f8f.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72655-02172655-021-04, 72655-021-05, 72655-021-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT

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
7f708256-5872-4f3e-ad44-e148229e52f44538f141-8055-4262-99d7-fe2cd9cc7f8f2020-04-09WarningsExact identifier
spl id: 7f708256-5872-4f3e-ad44-e148229e52f4
spl set id: 4538f141-8055-4262-99d7-fe2cd9cc7f8f

Reported adverse events (FAERS/openFDA)#

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