NDC 51270-115 Hasol Revitalizing Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51270-115?
What are the uses for Hasol Revitalizing Treatment?
Which are Hasol Revitalizing Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Hasol Revitalizing Treatment 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-3 (UNII: F32E4CB0UJ)
- LAURETH-23 (UNII: N72LMW566G)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- TOMATO (UNII: Z4KHF2C175)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TEA TREE OIL (UNII: VIF565UC2G)
- LYCOPENE (UNII: SB0N2N0WV6)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- CORNUS OFFICINALIS FRUIT (UNII: 23NL8NQ187)
- DIOSCOREA JAPONICA TUBER (UNII: I43FCF3356)
- ALISMA PLANTAGO-AQUATICA TOP (UNII: 321GB7FW2H)
- PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- FU LING (UNII: XH37TWY5O4)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ENGLISH WALNUT (UNII: 1V3SHR7QB7)
- POMEGRANATE (UNII: 56687D1Z4D)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SWERTIA JAPONICA (UNII: 01X0P6GX6C)
- SOYBEAN (UNII: L7HT8F1ZOD)
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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".