Antibacterial

Manufacturer
Sante Manufacturing Inc
Effective date
2025-01-07
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:51:11

Label at a glance#

ProductAntibacterial 2X
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride - 0.13%

OTC - PURPOSE SECTION

Purpose: Antibacterial

DOSAGE & ADMINISTRATION SECTION

Direction

  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse

WARNINGS SECTION

For external use only

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops

OTC - WHEN USING SECTION

When using this product

  • do not get it into eyes. If contact occurs, rinse eye thoroughly with water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Citric Acid, Glycerin, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow# 5 (Cl 19140), Red# 4 (Cl 14700)

INDICATIONS & USAGE SECTION

Uses for handwashing or decrease bacteria to the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Liquid Soap 2XAntibacterial Liquid Soap 2X

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN6
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD6
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY6
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71020-005-02Antibacterial2X2 in 1 PACKAGELIQUID26
71020-005-02Antibacterial2X1900 mL in 1 BOTTLELIQUID19006
71020-005-64Antibacterial2X1900 mL in 1 BOTTLE, PLASTICLIQUID19006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71020-005ANTIBACTERIAL 2X (BENZALKONIUM CHLORIDE) LIQUID [SANTE MANUFACTURING INC]6Current NDC, Legacy NDC, 3 package rows20250109_3e65e67d-c7d0-2fcb-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71020-00571020-005-64, 71020-005-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Antibacterial 2XBENZALKONIUM CHLORIDESante Manufacturing Inc3e65e67d-c7d0-2fcb-e054-00144ff8d46c2025-01-07WarningsExact identifier
ndc (package): 71020-005-64
ndc (package): 71020-005-02
ndc (product): 71020-005
ndc11 (package): 71020000502
ndc11 (package): 71020000564
spl id: 2b21974d-5b74-b7c9-e063-6394a90a8ec9
spl set id: 3e65e67d-c7d0-2fcb-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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