SANIRUS HAND SANITIZER

Manufacturer
Global Cosmetics (China) Company Limited
Effective date
2020-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:14

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

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
71650-00471650-004-01

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
0bb9c71d-25eb-4e62-958b-6605b8de5c6e256886b7-210a-447b-83f5-8daec9fef82f2023-03-31WarningsExact identifier
spl set id: 256886b7-210a-447b-83f5-8daec9fef82f

Reported adverse events (FAERS/openFDA)#

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