FDA.reportPublic FDA data

SANITAXE ANTIBACTERIAL AMBER HAND 27 FL OZ

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2020-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:31

Label at a glance#

ProductSANITAXE ANTIBACTERIAL AMBER HAND 27 FL OZ
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

Helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Pump onto wet hands Work into lather Wash hands, rinse and dry thoroughly.

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13 percent

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only. Do not ingest or swallow.

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

OTC - STOP USE SECTION

if 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

Do not use on children less than 2 months of age. Supervise use in children under 6 years of age to prevent accidental swallowing. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump onto wet hands
  • Work into lather
  • Wash hands, rinse and dry thoroughly.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropye Betaine, Sodium Cocoamphoacetate, PEG-150 Distearate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No.5, D&C Red No.40

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
76176-12476176-124-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C RED NO. 40WZB9127XOAIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C YELLOW NO. 5I753WB2F1MIACT

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
af511208-bae0-501d-e053-2a95a90aeae9af511208-bae1-501d-e053-2a95a90aeae92020-09-01WarningsExact identifier
spl id: af511208-bae0-501d-e053-2a95a90aeae9
spl set id: af511208-bae1-501d-e053-2a95a90aeae9

Reported adverse events (FAERS/openFDA)#

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