NDC 55910-246 Medicated Dandruff

NDC Product Code 55910-246

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 a product labeled by Dolgencorp.llc. The generic name of Medicated Dandruff is . The product's dosage form is and is administered via form.

Labeler Name: Dolgencorp.llc

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.