FDA.reportPublic FDA data

SANITAXE ANTIBACTERIAL AMBER HAND

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 00:24:38

Label at a glance#

ProductSANITAXE ANTIBACTERIAL AMBER HAND
Active ingredientCHLOROXYLENOL
Label structure11 sections

Indications and uses

for handwashing to eliminate bacterial and germs on the skin.

Dosage and administration

wet hands. Apply palmful to hands. Scrub thoroughly. Rinse.

Label contents#

Full prescribing information#

Drug Facts Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.1 percent

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to eliminate bacterial and germs on the skin.

Warnings

WARNINGS SECTION

For external use only.

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 develops and persists 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

wet hands. Apply palmful to hands. Scrub thoroughly. Rinse.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Glycerin, Sodium Chloride, Fragrance, Citric Acid, PEG-150 Distearate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Yellow No.5.

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 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-11876176-118-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM LAURYL SULFATE368GB5141JIACT
GLYCERINPDC6A3C0OXIACT
CHLOROXYLENOL0F32U78V2QACTIB
CITRIC ACID ACETATEDSO12WL7AUIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT

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
86ca5f10-e46b-8064-e053-2a91aa0ac28586ca5f10-e46a-8064-e053-2a91aa0ac2852019-01-01WarningsExact identifier
spl id: 86ca5f10-e46b-8064-e053-2a91aa0ac285
spl set id: 86ca5f10-e46a-8064-e053-2a91aa0ac285