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SoftCIDE-ES

Medically reviewed on July 24, 2017

Dosage form: liquid
Ingredients: CHLOROXYLENOL 12.604g in 100mL
Labeler: Erie Scientific, LLC
NDC Code: 55863-281

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

SoftCIDE-ES

Chloroxylenol 0.3% w/w

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

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

Handwash to help reduce bacteria that can potentially cause disease.

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. If swallowed, seek medical help or contact Poison Control immediately.

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.

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SOFTCIDE-ES 
softcide-es liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55863-281
Route of AdministrationTopicalDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL12.604 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
EDETATE SODIUM 
POTASSIUM HYDROXIDE 
TALL OIL 
COCONUT ACID 
SODIUM LAURYL SULFATE 
COCO DIISOPROPANOLAMIDE 
PHENOXYETHANOL 
SODIUM SULFATE 
SODIUM LAURETH SULFATE 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL ACETATE, DL- 
IODOPROPYNYL BUTYLCARBAMATE 
D&C RED NO. 33 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:55863-281-27800 mL in 1 BAG
2NDC:55863-281-32946 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/13/2013
Labeler - Erie Scientific, LLC (361605223)
Registrant - Kutol Products Company, Inc. (004236139)
Establishment
NameAddressID/FEIOperations
Kutol Products Company, Inc.004236139manufacture(55863-281), pack(55863-281), analysis(55863-281)

 
Erie Scientific, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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