NDC 63824-418 Clearasil Ultra 5 In 1 Exfoliating Wash

NDC Product Code 63824-418

NDC 63824-418-67

Package Description: 200 mL in 1 TUBE

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

NDC Product Information

Clearasil Ultra 5 In 1 Exfoliating Wash with NDC 63824-418 is a product labeled by Reckitt Benckiser Llc. The generic name of Clearasil Ultra 5 In 1 Exfoliating Wash is . The product's dosage form is and is administered via form.

Labeler Name: Reckitt Benckiser Llc

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.

  • WATER (UNII: 059QF0KO0R)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • CETYL BETAINE (UNII: E945X08YA9)
  • DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • ALCOHOL (UNII: 3K9958V90M)
  • STEARETH-21 (UNII: 53J3F32P58)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • STEARETH-2 (UNII: V56DFE46J5)
  • HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • DIMETHYL PALMITAMINE (UNII: 5E4QI660PW)
  • LAURYL ALCOHOL (UNII: 178A96NLP2)
  • MICA (UNII: V8A1AW0880)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • MAGNESIUM NITRATE (UNII: 77CBG3UN78)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • SODIUM SULFATE (UNII: 0YPR65R21J)
  • FERRIC FERROCYANIDE (UNII: TLE294X33A)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Reckitt Benckiser Llc
Labeler Code: 63824
Start Marketing Date: 01-01-2015 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: 12-31-2019 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.

Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

* Please review the disclaimer below.

Clearasil Ultra 5 In 1 Exfoliating Wash Product Label Images

Clearasil Ultra 5 In 1 Exfoliating Wash 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 by:Reckitt BenckiserParsippany, NJ07054-0224Made in USA

Active Ingredient

Salicylic acid 2.0%

Purpose

Acne medication

Use

For the treatment of acne

Warnings

For external use only

When Using This Product

  • Avoid contact with the eyes. If product gets into the eyes rinse thoroughly with water.using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one acne medication should be used unless directed by your doctor.limit use to the face and neck

Otc - Stop Use

Stop use and ask a doctor if skin or eye irritation develops

Otc - Keep Out Of Reach Of Children

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

Directions

  • Wet face and dispense product into hands, lather and massage gently onto face and neck, avoiding the eye areacover the entire affected area with a thin layer and rinse thoroughly with warm water one to three times dailybecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness occurs, reduce application to once a day or every other day

Other Information

  • Keep tightly closedstore in a cool, dry place

Inactive Ingredients

Water, polyethylene, PPG-15 stearyl ether, glycerin, stearyl alcohol, cetyl betaine, distearyldimonium chloride, sodium lauryl sulfate, cetyl alcohol, alcohol, steareth-21, sodium chloride, behenyl alcohol, synthetic wax, steareth-2, fragrance, Lavandula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract, xanthan gum, dimethyl palmitamine, lauryl alcohol, mica, isopropyl alcohol, disodium EDTA, BHT, magnesium nitrate, methylchloroisothiazolinone, magnesium chloride, methylisothiazolinone, sodium sulfate, ferric ferrocyanide, titanium dioxide, FD&C blue no. 1

Questions?

1-866-252-5327.

* Please review the disclaimer below.