NDC 55118-205 Scott Clear Antibacterial Skin Cleanser

NDC Product Code 55118-205

NDC 55118-205-05

Package Description: 500 mL in 1 BAG

NDC 55118-205-08

Package Description: 800 mL in 1 BAG

NDC 55118-205-10

Package Description: 1000 mL in 1 BAG

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Scott Clear Antibacterial Skin Cleanser with NDC 55118-205 is a product labeled by Kimberly-clark Corporation. The generic name of Scott Clear Antibacterial Skin Cleanser is . The product's dosage form is and is administered via form.

Labeler Name: Kimberly-clark Corporation

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • COCO DIETHANOLAMIDE (UNII: 92005F972D)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Kimberly-clark Corporation
Labeler Code: 55118
Start Marketing Date: 03-01-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Scott Clear Antibacterial Skin Cleanser Product Label Images

Scott Clear Antibacterial Skin Cleanser Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts

Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5

Active Ingredient

Triclosan 0.25%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin.

Warnings

For External Use Only.

Otc - When Using

When using this product avoid contact with eyes; in case of contact, flush eyes with water.

Otc - Ask Doctor

Stop use & ask a doctor if irritation or redness develops and persists.

Otc - Keep Out Of Reach Of Children

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

Directions

Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds. Rinse and dry thoroughly.

Other Information

  • Report serious side effects from this product to 1-877-561-6587

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Beteine, Glycerin, Propylene Glycol, Frangrance, DL-Panthenol, Aloe Barbadensis Leaf Juice, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Cocamide DEA.

Questions?

1-888-346-4652

* Please review the disclaimer below.