Sanitect Antibacterial Hand

Manufacturer
Aquagenics Technologies
Effective date
2023-07-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:28:07

Label at a glance#

ProductSanitect Antibacterial Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For handwashing , helps eliminate bacteria on hands.

Dosage and administration

Pump onto wet hands, vigorously work into a lather and rinse thoroughly.

Storage and handling

Store in a cool dry place below 104F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing , helps eliminate bacteria on hands.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if irritation or rash develops.

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

Stop use and ask doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump onto wet hands, vigorously work into a lather and rinse thoroughly.

Other information

STORAGE AND HANDLING SECTION

Store in a cool dry place below 104F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, lauramine Oxide, Cocamidopropyl Betaine, Coco Glucoside, Glycerin, Lavender Oil, Citric Acid, Methylchloroisothiazolinone.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Soap Front PanelSoap Front PanelSoap Drug FactsSoap Drug FactsNDC: 73763-466-01

FDA-Initiated Inactive NDC Indexing#

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
73763-46673763-466-01, 73763-466-02, 73763-466-03, 73763-466-04, 73763-466-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
28639d5f-1d73-953b-e063-6394a90adc5ba203e36d-f22e-cb45-e053-2a95a90a71882024-12-03WarningsExact identifier
spl set id: a203e36d-f22e-cb45-e053-2a95a90a7188

Reported adverse events (FAERS/openFDA)#

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