NDC 51270-123 Hasol Anagen Scalp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51270 - Ecomine Co., Ltd.
- 51270-123 - Hasol Anagen Scalp
Product Packages
NDC Code 51270-123-02
Package Description: 1 BOTTLE in 1 PACKAGE / 500 g in 1 BOTTLE (51270-123-01)
Product Details
What is NDC 51270-123?
Which are Hasol Anagen Scalp UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- DEXPANTHENOL (UNII: 1O6C93RI7Z) (Active Moiety)
Which are Hasol Anagen Scalp 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)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
- GLYCERIN (UNII: PDC6A3C0OX)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SALVIA OFFICINALIS ROOT (UNII: 236QY0A1BL)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- GINGER (UNII: C5529G5JPQ)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- JOJOBA OIL (UNII: 724GKU717M)
- ETHYLHEXYL COCOATE (UNII: I1MPW273QS)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BETAINE (UNII: 3SCV180C9W)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
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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".