Label at a glance#

ProductTRICLOSAN

Active ingredientTRICLOSAN

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose
Triclosan 0.25%...............................Antiseptic

OTC - PURPOSE SECTION

Active ingredient Purpose

Triclosan 0.25%...............................Antiseptic

Use to decrease bacteria on the skin

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 Immediately.

INDICATIONS & USAGE SECTION

Directions mix in hands with water. Work into a foamy lather.

Smooth over face and neck. Rinse thoroughly.

WARNINGS SECTION

Warnings For external use only.

Stop use and ask a doctor if

- excessive skin irritation develops or condition worsens
- symptoms last more than 7 days or clear up and occur
again within a few days.

Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center Immediately.

DOSAGE & ADMINISTRATION SECTION

Directions
- Mix in hands with water. Work into a foamy lather.
Smooth over face and neck. Rinse thoroughly.

Other Information do not store in a location where water may enter the bottle

INACTIVE INGREDIENT SECTION

Inactive Ingredients BHT, Butylparaben, C9-15 Alkyl Phosphate,
Cocamidopropyl Bataine, Ethylparaben, Fragrance, Glycerin,
Hydroxypropyl Methylcelluose, Lauric Acid, Methylparaben, Myristic Acid,
Phenoxyethanol, Propylparaben, Triethanolamine, Water, Red 40, Yellow 10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
831578	triclosan 0.25 % Medicated Liquid Soap	PSN	2
831578	triclosan 2.5 MG/ML Medicated Liquid Soap	SCD	2
831578	triclosan 0.25 % Medicated Liquid Soap	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59779-081-20	2019-10-29	C162847	48780-1	960f7f55-db1d-8e05-e053-dbdaa90a074a	drug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-081-20	TRICLOSAN	240 mL in 1 BOTTLE	LIQUID	240		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-081	TRICLOSAN LIQUID [CVS PHARMACY]	2	Legacy NDC, 1 package rows	20110720_92594681-2f84-4638-b506-1ecf46b64928.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	2
UNDECYLENIC ACID	ACTIVE MOIETY	K3D86KJ24N	2
ISOPROPYL PALMITATE	INACTIVE INGREDIENT	8CRQ2TH63M	2

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

TRICLOSAN
UNDECYLENIC ACID
ISOPROPYL PALMITATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59779-081	59779-081-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TRICLOSAN	4NM5039Y5X	ACTIB
ISOPROPYL PALMITATE	8CRQ2TH63M	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	FILM / TRANSDERMAL		2 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	AEROSOL / TOPICAL		397 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	FILM, EXTENDED RELEASE / TRANSDERMAL	187.5 mg		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	GEL / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	LOTION / TOPICAL	5 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	CREAM / TOPICAL		112 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
ISOPROPYL PALMITATE	ISOPROPYL PALMITATE	8CRQ2TH63M	AEROSOL, SPRAY / TOPICAL		397 mg	Exact identifier — unii candidate 8 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
4806c610-7f72-49cc-9419-7b6bd264d171			92594681-2f84-4638-b506-1ecf46b64928	2011-02-16	Warnings	Exact identifier spl id: 4806c610-7f72-49cc-9419-7b6bd264d171 spl set id: 92594681-2f84-4638-b506-1ecf46b64928

Reported adverse events (FAERS/openFDA)#

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