SoftCIDE-ES by Erie Scientific, LLC / Kutol Products Company, Inc. SOFTCIDE-ES liquid

SoftCIDE-ES by

Drug Labeling and Warnings

SoftCIDE-ES by is a Otc medication manufactured, distributed, or labeled by Erie Scientific, LLC, Kutol Products Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Chloroxylenol 0.3% w/w

INACTIVE INGREDIENT

Water, Tall Oil Acid, Potassium Hydroxide, Sodium Lauryl Sulfate, Coconut Acid, Cocamide DIPA, Phenoxyethanol, Tetrasodium EDTA, Sodium Sulfate, Sodium Laureth Sulfate, Aloe Barbadensis Leaf, Tocopheryl Acetate (Vitamin E Acetate), Iodopropynyl Butylcarbamate, Fragrance, Red 33, Yellow 5

DOSAGE & ADMINISTRATION

Wet skin and apply a sufficient amount on hands and forearms. Scrub well and rinse thoroughly after washing.

PURPOSE

Handwash to help reduce bacteria that can potentially cause disease.

INDICATIONS & USAGE

Handwash to help reduce bacteria that can potentially cause disease.

Avoid contact with the eyes. If contact occurs, flush eyes with water.

Discontinue use and consult a health practitioner if irritation develops. If swallowed seek medical help or contact Posion Control immediately. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, seek medical help or contact Poison Control immediately.

WARNINGS

Avoid contact with eyes. If contact occurs, flush eyes with water.

For external use only.

Avoid contact with the eyes. If contact occurs, flush eyes with water.

Discontinue use and consult a health practitioner if irritation develops.

If swallowed seek medical help or contact Posion Control immediately.

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

55863-281-27-ERI.jpg

PRINCIPAL DISPLAY PANEL

55863-281-32-ERI.jpg

PRINCIPAL DISPLAY PANEL

55863-281-32-VWR.jpg

PRINCIPAL DISPLAY PANEL

55863-281-27-VWR.jpg

INGREDIENTS AND APPEARANCE

SOFTCIDE-ES 
softcide-es liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55863-281
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	12.604 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
TALL OIL (UNII: 1GX6Z36A79)
COCONUT ACID (UNII: 40U37V505D)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM SULFATE (UNII: 0YPR65R21J)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55863-281-27	800 mL in 1 BAG
2	NDC: 55863-281-32	946 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/13/2013

Labeler - Erie Scientific, LLC (361605223)

Registrant - Kutol Products Company, Inc. (004236139)

Establishment
Name	Address	ID/FEI	Business Operations
Kutol Products Company, Inc.		004236139	manufacture(55863-281) , pack(55863-281) , analysis(55863-281)