NDC 55910-246 Medicated Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55910 - Dolgencorp.llc
- 55910-246 - Medicated Dandruff
Product Packages
NDC Code 55910-246-39
Package Description: .325 L in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55910-246?
What are the uses for Medicated Dandruff?
Which are Medicated Dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- SELENIUM SULFIDE (UNII: Z69D9E381Q)
- SELENIUM SULFIDE (UNII: Z69D9E381Q) (Active Moiety)
Which are Medicated Dandruff Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- 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)
What is the NDC to RxNorm Crosswalk for Medicated Dandruff?
- RxCUI: 204642 - selenium sulfide 1 % Medicated Shampoo
- RxCUI: 204642 - selenium sulfide 10 MG/ML Medicated Shampoo
- RxCUI: 204642 - selenium sulfide 1 % Lotion Shampoo
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".