NDC 63214-102 Therapytion Nokmosu Neutral And Oily Hair
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63214 - Therapytion Co., Ltd.
- 63214-102 - Therapytion Nokmosu Neutral And Oily Hair
Product Packages
NDC Code 63214-102-02
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 530 g in 1 BOTTLE, PLASTIC (63214-102-01)
Product Details
What is NDC 63214-102?
Which are Therapytion Nokmosu Neutral And Oily Hair UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
Which are Therapytion Nokmosu Neutral And Oily Hair 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
- SOYBEAN (UNII: L7HT8F1ZOD)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SWERTIA JAPONICA (UNII: 01X0P6GX6C)
- GLYCYRRHIZA GLABRA WHOLE (UNII: M1F96IE0ZC)
- PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- BENZOPHENONE-9 (UNII: 7925W14T4L)
- CARAMEL (UNII: T9D99G2B1R)
* 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".