SANIRUS HAND SANITIZER

Manufacturer
6A Holding, LLC
Effective date
2020-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:11

Label at a glance#

ProductSANIRUS HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information • Store between 15°-30°C (59°-86°F). • May discolor fabrics

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses: Hand Sanitizer to help reduce bacteria on skin

WARNINGS SECTION

Warnings: For external use only.

Flammable. keep away from heat or flame.

When using this product • Avoid contact with eyes. In case of contact rinse with water.  • Do not inhale or ingest. • Avoid contact with broken skin.

Stop use and ask a doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

DOSAGE & ADMINISTRATION SECTION

Directions • Wet hands thoroughly and rub together until dry. • Adult supervision for children under 6. • Not for infants.

STORAGE AND HANDLING SECTION

Other information • Store between 15°-30°C (59°-86°F). • May discolor fabrics

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Butylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Triethanolamine, Citric Acid.

SPL UNCLASSIFIED SECTION

KILLS MOST OF THE GERMS

65% ALCOHOL

ALOE VERA

2X SANITIZING STRENGTH

REFRESHING GEL

GMP Quality

DISTRIBUTED BY: 6A HOLDING LLC, MIAMI, FLORIDA

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902574ethanol 65 % Topical GelPSN1
902574ethanol 0.65 ML/ML Topical GelSCD1
902574ethyl alcohol 65 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74691-002-022022-01-28C16284748780-1d6a99b39-a8ff-a426-e053-dadaa90af4c2Sanirus Hand Sanitizer 65

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74691-002-02SANIRUS HAND SANITIZER60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74691-002SANIRUS HAND SANITIZER (ETHYL ALCOHOL) GEL [6A HOLDING, LLC]1Legacy NDC, 1 package rows20200611_a7c03d82-57b1-83b8-e053-2a95a90a0bc8.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74691-00274691-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a7c04234-6cd5-189f-e053-2995a90a8851a7c03d82-57b1-83b8-e053-2a95a90a0bc82020-06-08WarningsExact identifier
spl id: a7c04234-6cd5-189f-e053-2995a90a8851
spl set id: a7c03d82-57b1-83b8-e053-2a95a90a0bc8

Reported adverse events (FAERS/openFDA)#

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