Sanitaxe Antibacterial

Manufacturer
American Consumer Products Corp
Effective date
2025-01-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:37

Label at a glance#

ProductSanitaxe Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride .13%

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Warnings – For external use only. Do not ingest or swallow.

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor 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

Keep out of reach of children. 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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Cocamidopropyl Betaine, Sodium Cocoamphoacetate, PEG-150 Disterate, Fragrance, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, FD&C Yellow No. 5, D&C Red No. 33.

Sanitaxe Hand Soap

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanitax Hand SoapSanitax Hand Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-033-27Sanitaxe Antibacterial800 mL in 1 BOXGEL8003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-033SANITAXE ANTIBACTERIAL (BENZALKONIUM CHLORIDE) GEL [AMERICAN CONSUMER PRODUCTS CORP]3Current NDC, Legacy NDC, 1 package rows20250125_a9ca8aaa-ea76-7eb5-e053-2995a90adef9.zip

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
72197-03372197-033-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Sanitaxe AntibacterialBENZALKONIUM CHLORIDEAmerican Consumer Products Corpa9ca8aaa-ea76-7eb5-e053-2995a90adef92025-01-23WarningsExact identifier
ndc (package): 72197-033-27
ndc (product): 72197-033
ndc11 (package): 72197003327
spl id: 2c69e7d6-d471-6723-e063-6294a90aa037
spl set id: a9ca8aaa-ea76-7eb5-e053-2995a90adef9

Reported adverse events (FAERS/openFDA)#

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