NDC 51270-120 Hasol Intensive Scalp Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51270 - Ecomine Co., Ltd.
- 51270-120 - Hasol Intensive Scalp Tonic
Product Packages
NDC Code 51270-120-02
Package Description: 1 BOTTLE in 1 CARTON / 100 mL in 1 BOTTLE (51270-120-01)
Product Details
What is NDC 51270-120?
Which are Hasol Intensive Scalp Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Hasol Intensive Scalp Tonic 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)
- ALCOHOL (UNII: 3K9958V90M)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- BETAINE (UNII: 3SCV180C9W)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- GINGER (UNII: C5529G5JPQ)
- LAMINARIA JAPONICA (UNII: WE98HW412B)
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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".