Signature Home AB Orange

Manufacturer: Sun Products Corporation | Safeway
Effective date: 2016-06-29
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:46:26

Label at a glance#

ProductSignature Home AB Orange

Active ingredientCHLOROXYLENOL

Label structure10 sections

Dosage and administration

wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Contacts and useful links#

PhoneLabel contact1-888-723-3929

Label contents#

Full prescribing information#

Dishwashing Liquid & Antibacterial Hand Soap

STATEMENT OF IDENTITY SECTION

ULTRA Concentrated

orange scent

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.30%

Purpose

OTC - PURPOSE SECTION

Antibacterial hand soap

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Didecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Sodium Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, D&C Red No. 33

Questions?

OTC - QUESTIONS SECTION

Questions? 1-888-723-3929

Signature Home Orange AB-page-001.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Signature Home Orange AB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
413261	chloroxylenol 0.3 % Medicated Liquid Soap	PSN	1
413261	chloroxylenol 3 MG/ML Medicated Liquid Soap	SCD	1
413261	chloroxylenol 0.3 % Medicated Liquid Soap	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63691-027-10	2020-01-31	C162847	48780-1	9d75b9d0-15f1-f424-e053-dadaa90a57ce	367183cb-ccaa-38c8-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63691-027-10	Signature Home AB Orange	709 mL in 1 BOTTLE	SOAP	709		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63691-027	SIGNATURE HOME AB ORANGE (CHLOROXYLENOL) SOAP [SUN PRODUCTS CORPORATION]	1	Legacy NDC, 1 package rows	20160630_367183cb-ccaa-38c8-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Signature Home AB Orange
Chloroxylenol
SODIUM XYLENESULFONATE
SODIUM LAURYL SULFATE
SODIUM LAURETH SULFATE
ALCOHOL
EDETATE SODIUM
METHYLCHLOROISOTHIAZOLINONE
FD&C YELLOW NO. 5
D&C RED NO. 33
WATER
BENZISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
SODIUM DODECYLBENZENESULFONATE
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63691-027	63691-027-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM XYLENESULFONATE	G4LZF950UR	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
ALCOHOL	3K9958V90M	IACT
EDETATE SODIUM	MP1J8420LU	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
D&C RED NO. 33	9DBA0SBB0L	IACT
WATER	059QF0KO0R	IACT
BENZISOTHIAZOLINONE	HRA0F1A4R3	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
SODIUM DODECYLBENZENESULFONATE	554127163Y	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB

Source Document#

Source XML · Source PDF

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
367183cb-ccab-38c8-e054-00144ff88e88			367183cb-ccaa-38c8-e054-00144ff88e88	2016-06-29	Warnings	Exact identifier spl id: 367183cb-ccab-38c8-e054-00144ff88e88 spl set id: 367183cb-ccaa-38c8-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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