NDC 55910-246 Medicated Dandruff

  1. Labeler Index
  2. Dolgencorp.llc
  3. NDC: 55910-246 Medicated Dandruff

NDC Product Code 55910-246

NDC CODE: 55910-246

Proprietary Name: Medicated Dandruff What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as purposeanti-dandruff

NDC Code Structure

NDC 55910-246-39

Package Description: .325 L 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

Medicated Dandruff with NDC 55910-246 is product labeled by Dolgencorp.llc. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:


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-3 SULFATE (UNII: 896SJ235FN)
  • 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)
  • HYPROMELLOSES (UNII: 3NXW29V3WO)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

Product Labeler Information

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

Labeler Name: Dolgencorp.llc
Labeler Code: 55910
Start Marketing Date: 11-03-2011 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

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]

* Please review the disclaimer below.

Medicated Dandruff Product Label Images

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

Otc - Active Ingredient

Active ingredientSelenium sulfide 1%

Otc - Purpose

PurposeAnti-Dandruff

Indications & Usage

Use for relief of itching and flaking associated with dandruff and seborrheic dermatitis and to help prevent reoccurrence

Warnings

WarningsFor external use only

Otc - Ask Doctor

Ask a doctor before use if you have seborrheic dermatitis in areas other than the scalp

Otc - When Using

When using this product •do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if  •condition worsens or does not improve after regular use as directed

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

Directions •Shake well •wet hair, massage onto scalp, rinse thoroughly •for best results use at least twice a week or as directed b a doctor

Other Safety Information

Other information for color-treated or permed hair, rinse extra thoroughly

Inactive Ingredient

Inactive ingredients water, ammonium laury sulfate, TEA-lauryl sulfate, ammonium laureth sulfate,  cocamidopropyl betaine, magnesium aluminum silicate, fragrance,menthol, cocamide DEA, DMDM hydantoin citric acid, hydroxypropyl methylcellulose, xanthan gum, cellulose gum, FD+C blue no. 1, D+C red no 33, sodium citrate, sodium chloride.

Adverse Reactions

PACKAGED FOR DOLGENCORP, LLC100 MISSION RIDGE, GOODLETTSVILLE, TN 37072 USAvisit us at Rexall.com or call 1-866-4-REXALL

* Please review the disclaimer below.