FDA.reportPublic FDA data

SANITAXE INSTANT HAND SANITIZER WITH ALOE VERA 27 FL OZ

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2019-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:48

Label at a glance#

ProductSANITAXE INSTANT HAND SANITIZER WITH ALOE VERA 27 FL OZ
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. when water, soap and towel are not available. recommended for repeated use.

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands, rub into skin until dry.

Label contents#

Full prescribing information#

Drug Facts Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62 percent

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin.
  • when water, soap and towel are not available.
  • recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears and mouth.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands, rub into skin until dry.

Other information

OTHER SAFETY INFORMATION

  • store at 20 Degree Celsius (68 to 77 Fahrenheit).
  • may discolor fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, aloe barbadensis gel, carbomber, fragrance.

Loading Instructions

ASSEMBLY OR INSTALLATION INSTRUCTIONS

1. Tear tab off of box and pull out tube. Pull down nozzle until tube extends from bottom of box.

2. Place Bag-In-Box into dispenser. Guide nozzle fitment into valve channel and close dispenser. Push button to prime.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-11976176-119-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 934Z135WT9208IACT
TRIETHANOLAMINE BENZOATEM3EN4GC19WIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB

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
868d29c5-b040-91fc-e053-2a91aa0a608f868d29c5-b03f-91fc-e053-2a91aa0a608f2019-01-01WarningsExact identifier
spl id: 868d29c5-b040-91fc-e053-2a91aa0a608f
spl set id: 868d29c5-b03f-91fc-e053-2a91aa0a608f

Reported adverse events (FAERS/openFDA)#

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