UP (AND) UP GREEN APPLE SCENT- chloroxylenol soap

Up (and) Up Green Apple Scent by

Drug Labeling and Warnings

Up (and) Up Green Apple Scent by is a Otc medication manufactured, distributed, or labeled by Sun Products Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chloroxylenol 0.30%

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

Purpose

Antibacterial hand soap

Inactive ingredients

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

QUESTIONS

Questions? 1-800-910-6874

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

INGREDIENTS AND APPEARANCE

UP (AND) UP GREEN APPLE SCENT 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63691-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
EDETATE SODIUM (UNII: MP1J8420LU)
BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
WATER (UNII: 059QF0KO0R)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63691-029-30	1774 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2015
2	NDC: 63691-029-10	709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/30/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/30/2015

Labeler - Sun Products Corporation (070931480)