NDC 55910-621 Rexall Aloe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55910 - Dolgencorp Inc
- 55910-621 - Rexall
Product Packages
NDC Code 55910-621-11
Package Description: 325 mL in 1 BOTTLE, PLASTIC
NDC Code 55910-621-12
Package Description: 325 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55910-621?
What are the uses for Rexall Aloe?
Which are Rexall 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 Rexall 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)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Rexall 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.
[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".