NDC 41520-623 Careone Moisturizing Dandruff With Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 41520-623?
What are the uses for Careone Moisturizing Dandruff With Aloe?
Which are Careone Moisturizing Dandruff With Aloe 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 Careone Moisturizing Dandruff With Aloe 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)
- DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Careone Moisturizing Dandruff With Aloe?
- 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.
[Learn More]
* 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".