NDC 66854-017 Spai-sons Alkaline Dry-dandruff
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What is NDC 66854-017?
What are the uses for Spai-sons Alkaline Dry-dandruff?
Which are Spai-sons Alkaline Dry-dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Spai-sons Alkaline Dry-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)
- DIHYDROGENATED TALLOW PHTHALIC ACID AMIDE (UNII: 1R81RPY10G)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- TROLAMINE (UNII: 9O3K93S3TK)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PONCEAU 4R (UNII: Z525CBK9PG)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
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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".