NDC 63148-005 Shopko Beauty Maximum Strength Medicated Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63148 - Apollo Health And Beauty Care Inc.
- 63148-005 - Shopko Beauty Maximum Strength Medicated Dandruff
Product Packages
NDC Code 63148-005-11
Package Description: 325 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63148-005?
What are the uses for Shopko Beauty Maximum Strength Medicated Dandruff?
Which are Shopko Beauty Maximum Strength 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 Shopko Beauty Maximum Strength 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- TRIETHANOLAMINE LAURYL SULFATE (UNII: E8458C1KAA)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- MENTHOL (UNII: L7T10EIP3A)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Shopko Beauty Maximum Strength 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.
Patient Education
Selenium Sulfide
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 seborrhea. It is also used to treat tinea versicolor, a fungal infection of the skin. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* 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".