NDC 66854-021 Spai-sons Acid Anti-dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66854 - Spai-sons Pharamcuetical International Cosmetics
- 66854-021 - Spai-sons
Product Packages
NDC Code 66854-021-01
Package Description: 210 mL in 1 BOTTLE
NDC Code 66854-021-02
Package Description: 250 mL in 1 BOTTLE
NDC Code 66854-021-03
Package Description: 250 mL in 1 BOTTLE
Product Details
What is NDC 66854-021?
What are the uses for Spai-sons Acid Anti-dandruff?
Which are Spai-sons Acid Anti-dandruff UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Spai-sons Acid 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- LAURETH-10 (UNII: BD7AST04GA)
- DIPYRITHIONE (UNII: 9L87N86R9A)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TROLAMINE (UNII: 9O3K93S3TK)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".