NDC 11822-4500 Renewal Anti-dandruff
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11822-4500?
What are the uses for Renewal Anti-dandruff?
Which are Renewal Anti-dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Renewal Anti-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)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE SODIUM (UNII: MP1J8420LU)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Renewal Anti-dandruff?
- RxCUI: 205104 - salicylic acid 2 % Medicated Shampoo
- RxCUI: 205104 - salicylic acid 20 MG/ML Medicated Shampoo
- RxCUI: 205104 - salicylic acid 2 % Medicated Conditioner
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[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".