NDC 11822-6101 Rite Aid Medicated Dandruff

NDC Product Code 11822-6101

NDC 11822-6101-1

Package Description: 325 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Rite Aid Medicated Dandruff with NDC 11822-6101 is a product labeled by Rite Aid Corporation. The generic name of Rite Aid Medicated Dandruff is . The product's dosage form is and is administered via form.

Labeler Name: Rite Aid 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.

  • WATER (UNII: 059QF0KO0R)
  • AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
  • TROLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
  • AMMONIUM LAURETH-5 SULFATE (UNII: 43ZIH89I48)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
  • MENTHOL (UNII: L7T10EIP3A)
  • COCO DIETHANOLAMIDE (UNII: 92005F972D)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • 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: Rite Aid Corporation
Labeler Code: 11822
Start Marketing Date: 09-29-2010 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: 12-31-2018 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’.

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Information for Patients

Selenium Sulfide

Selenium Sulfide is pronounced as (se lee' nee um)

Why is selenium sulfide medication prescribed?
Selenium sulfide, an anti-infective agent, relieves itching and flaking of the scalp and removes the dry, scaly particles that are commonly referred to as dandruff or seb...
[Read More]

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Rite Aid Medicated Dandruff Product Label Images

Rite Aid Medicated Dandruff 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

Active Ingredient

SELENIUM SULFIDE 1%

Purpose

  • ANTI DANDRUFF

Warnings

  • FOR EXTERNAL USE ONLY.

Ask A Doctor Before Using If You Have

SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP

When Using This Product

  • AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. FOR USE ON COLOR-TREATED OR PERMED HAIR, RINSE THOROUGHLY.

Stop Use And Ask A Doctor If

  • CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED.

Keep Out Of Reach Of Children

  • IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

Use

FOR RELIEF OF FLAKING AND ITCHING DUE TO DANDRUFF, AND SEBORRHEIC DERMATITIS, AND TO HELP PREVENT THE CHANCE OF RE-OCCURRENCE.

Directions

  • SHAKE WELL, SHAMPOO, THEN RINSE THROUGHLY.FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR.

Inactive Ingredients

WATER, AMMONIUM LAURYL SULFATE, TEA-LAURYL SULFATE, AMMONIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, MAGNESIUM ALUMINUM SILICATE, FRAGRANCE, MENTHOL, COCAMIDE DEA, DMDM HYDANTOIN, CITRIC ACID, HYDROXYPROPYL METHYLCELLULOSE, SODIUM CITRATE, SODIUM CHLORIDE, BLUE 1 (CI 42090), RED 33 (CI 17200)

Package Front And Back Labels

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