Up (and) Up Green Apple Scent

Manufacturer: Sun Products Corporation
Effective date: 2016-06-30
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:46:26

Label at a glance#

ProductUp (and) Up Green Apple Scent

Active ingredientCHLOROXYLENOL

Label structure9 sections

Contacts and useful links#

PhoneLabel contact1-800-910-6874

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.30%

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

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.

DOSAGE & ADMINISTRATION SECTION

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

Purpose

OTC - PURPOSE SECTION

Antibacterial hand soap

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Soidum Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, FD&C Blue No. 1

OTC - QUESTIONS SECTION

Questions? 1-800-910-6874

Target 60oz GAAB LDU 690004755_690005736-page-001.jpg Target 24oz GAAB LDU 4900008630_4900008631-page-001.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Target 24 ozUP(and)UP GAAB

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
413261	chloroxylenol 0.3 % Medicated Liquid Soap	PSN	2
413261	chloroxylenol 3 MG/ML Medicated Liquid Soap	SCD	2
413261	chloroxylenol 0.3 % Medicated Liquid Soap	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63691-029-10	2020-01-31	C162847	48780-1	9d75b9d0-9a1b-f424-e053-dadaa90a57ce	27fa2840-adae-045a-e054-00144ff8d46c
63691-029-30	2020-01-31	C162847	48780-1	9d75b9d0-9a1b-f424-e053-dadaa90a57ce	27fa2840-adae-045a-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63691-029-10	Up (and) Up Green Apple Scent	709 mL in 1 BOTTLE, PLASTIC	SOAP	709		2
63691-029-30	Up (and) Up Green Apple Scent	1774 mL in 1 BOTTLE	SOAP	1774		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63691-029	UP (AND) UP GREEN APPLE SCENT (CHLOROXYLENOL) SOAP [SUN PRODUCTS CORPORATION]	2	Legacy NDC, 2 package rows	20160630_27fa2840-adae-045a-e054-00144ff8d46c.zip

Products#

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

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

Up (and) Up Green Apple Scent
Chloroxylenol
SODIUM LAURETH SULFATE
SODIUM XYLENESULFONATE
EDETATE SODIUM
BENZISOTHIAZOLINONE
WATER
SODIUM DODECYLBENZENESULFONATE
SODIUM CHLORIDE
ALCOHOL
SODIUM LAURYL SULFATE
METHYLISOTHIAZOLINONE
METHYLCHLOROISOTHIAZOLINONE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63691-029	63691-029-30, 63691-029-10

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 LAURETH SULFATE	BPV390UAP0	IACT
SODIUM XYLENESULFONATE	G4LZF950UR	IACT
EDETATE SODIUM	MP1J8420LU	IACT
BENZISOTHIAZOLINONE	HRA0F1A4R3	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
SODIUM DODECYLBENZENESULFONATE	554127163Y	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
ALCOHOL	3K9958V90M	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT

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
3680e9c4-c93f-60a6-e054-00144ff88e88			27fa2840-adae-045a-e054-00144ff8d46c	2016-06-30	Warnings	Exact identifier spl id: 3680e9c4-c93f-60a6-e054-00144ff88e88 spl set id: 27fa2840-adae-045a-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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