FDA.reportPublic FDA data

Antibacterial

Manufacturer
Sante Manufacturing Inc
Effective date
2016-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:47:47

Label at a glance#

ProductAntibacterial
Active ingredientTRICLOSAN
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient - Triclosan 0.115%

OTC - PURPOSE SECTION

Purpose - Antibacterial

INDICATIONS & USAGE SECTION

Uses for handwashing to decrease bacteria on the skin

WARNINGS SECTION

Warning for external use only

OTC - STOP USE SECTION

Stop us and ask a doctor if irritation or redness develops

OTC - WHEN USING SECTION

When using this product do not get 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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wet Hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Chloride, DMDM Hydantoin, Citric Acid, Fragrance, EDTA, Yellow#5, Red# 33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Spa Soap Anitibacterial 1XSpa Soap Anitibacterial 1X

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
995367triclosan 0.115 % Medicated Liquid SoapPSN2
995367triclosan 1.15 MG/ML Medicated Liquid SoapSCD2
995367triclosan 0.115 % Medicated Liquid SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71020-008-642020-01-31C16284748780-19d75b9d0-b980-f424-e053-dadaa90a57ce3f3a9b76-4a2a-4aaa-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71020-008-64Antibacterial1900 mL in 1 BOTTLELIQUID19002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71020-008ANTIBACTERIAL (TRICLOSAN) LIQUID [SANTE MANUFACTURING INC]2Legacy NDC, 1 package rows20161026_3f3a9b76-4a2a-4aaa-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71020-00871020-008-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRICLOSAN4NM5039Y5XACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
DMDM HYDANTOINBYR0546TOWIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
EDETIC ACID9G34HU7RV0IACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 3PN2ZH5LOQYIACT

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
3fc568c2-05bf-283e-e054-00144ff8d46c3f3a9b76-4a2a-4aaa-e054-00144ff88e882016-10-26WarningsExact identifier
spl id: 3fc568c2-05bf-283e-e054-00144ff8d46c
spl set id: 3f3a9b76-4a2a-4aaa-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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