FDA.reportPublic FDA data

HYR Hand Sanitizer

Manufacturer
General Resources LLC
Effective date
2020-10-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:43

Label at a glance#

ProductHYR Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Storage and handling

Other information Store above 0°C (32°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

Hand sanitizing to help reduce bacteria on the skin

WARNINGS SECTION

Warnings

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

​Stop use and ask a doctor if irritation or redness appears and lasts

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply liberally to the hands and gently rub until dry.

STORAGE AND HANDLING SECTION

Other information

Store above 0°C (32°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

purified water

SPL UNCLASSIFIED SECTION

Distributed by: General Resources, LLC

227 S. Smith Rd, Suite 102, Tempe, AZ 85281

www.gen-resources.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HYR

hand sanitizer

INSTANTLY KILLS 99.99% of OF TESTED GERMS

8 fl oz (236 mL)

Proudly made in the USA

70481-300 label 10-2070481-300 label 10-20

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN2
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD2
1049254benzalkonium chloride 0.13 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70481-300-062022-01-28C16284748780-1d6a99b39-635c-a426-e053-dadaa90af4c2HYR Hand Sanitizer
70481-300-242022-01-28C16284748780-1d6a99b39-635c-a426-e053-dadaa90af4c2HYR Hand Sanitizer
70481-300-262022-01-28C16284748780-1d6a99b39-635c-a426-e053-dadaa90af4c2HYR Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70481-300-06HYR Hand Sanitizer60 mL in 1 BOTTLE, SPRAYLIQUID602
70481-300-24HYR Hand Sanitizer237 mL in 1 BOTTLE, SPRAYLIQUID2372
70481-300-26HYR Hand Sanitizer3800 mL in 1 JUGLIQUID38002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70481-300HYR HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [GENERAL RESOURCES LLC]2Legacy NDC, 3 package rows20201016_a27b10ac-08f2-1ffa-e053-2a95a90aa66d.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70481-30070481-300-24, 70481-300-06, 70481-300-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

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
b1ba5f9b-b967-9326-e053-2a95a90ad798a27b10ac-08f2-1ffa-e053-2a95a90aa66d2020-10-15WarningsExact identifier
spl id: b1ba5f9b-b967-9326-e053-2a95a90ad798
spl set id: a27b10ac-08f2-1ffa-e053-2a95a90aa66d

Reported adverse events (FAERS/openFDA)#

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