Label at a glance#

ProductAntibacterial SUNBLOSSOM

Active ingredientTRICLOSAN

Label structure7 sections

Indications and uses

For washing to decrease bacteria on the skin.

Dosage and administration

Apply onto wet hands, work into a lather. Rinse thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Triclosan 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

- Avoid contact with eyes. If contact occurs, rinse with water.

Stop using this product and ask doctor if

OTC - STOP USE SECTION

- Irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on the skin.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply onto wet hands, work into a lather. Rinse thoroughly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Acrylates Copolymer, Cocamidopropyl Betaine, Cocamide DEA, Sodium Chloride, Fragrance (Parfum), Aloe Barbadensis Leaf Juice, PEG-7 Glyceryl Cocoate, Helianthus Annuus (Sunflower) Seed Extract, Tetrasodium EDTA, Sodium Styrene/PEG-10 Maleate/Nonoxynol-10 Maleate/ Acrylates Copolymer, Ammonium Nonoxynol-4 Sulfate, Citric Acid, Sodium Hydroxide, Mannitol, Cellulose, Tocopheryl Acetate, Hydroxypropyl Methylcellulose, Mica, Titanium Oxide (CI 77891), Yellow 10 (CI 47005), Red 40 (CI 16035), Iron Oxides ( CI 77492), Methylchloroisothiazolinone, Methylisothiazolinone.

PACKAGE FRONT AND BACK LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8.5 OZ Front Panel Label: eobf.jpg8.5OZ Front Panel Label
8.5 OZ Back Panel Label: eobb.jpg8.5 OZ Back Panel Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
260054	triclosan 0.3 % Medicated Liquid Soap	PSN	1
260054	triclosan 3 MG/ML Medicated Liquid Soap	SCD	1
260054	triclosan 0.3 % Foaming Medicated Hand Soap	SY	1
260054	triclosan 0.3 % Medicated Liquid Soap	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59779-284-09	2020-01-31	C162847	48780-1	9d75b9d1-0cb4-f424-e053-dadaa90a57ce	Drug Facts Box - Back Panel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-284-09	AntibacterialSUNBLOSSOM	251.00 mL in 1 BOTTLE, PUMP	SOAP	251.00		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-284	ANTIBACTERIAL SUNBLOSSOM (TRICLOSAN) SOAP [CVS PHARMACY ]	1	Legacy NDC, 1 package rows	20100831_8abc1ead-3e4e-4e5a-8e59-8f043bb20bb9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	1
TRICLOSAN	ACTIVE MOIETY	4NM5039Y5X	1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Antibacterial SUNBLOSSOM
Triclosan

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59779-284	59779-284-09

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
TRICLOSAN	4NM5039Y5X	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
7fcc142e-92c6-4b88-af2c-55052c72b53c			8abc1ead-3e4e-4e5a-8e59-8f043bb20bb9	2010-08-24	Warnings	Exact identifier spl id: 7fcc142e-92c6-4b88-af2c-55052c72b53c spl set id: 8abc1ead-3e4e-4e5a-8e59-8f043bb20bb9

Reported adverse events (FAERS/openFDA)#

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