NDC 51270-111 Hesol Rim
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51270 - Ecomine Co Ltd
- 51270-111 - Hesol Rim
Product Characteristics
Product Packages
NDC Code 51270-111-02
Package Description: 1 BOTTLE in 1 BOX / 300 mL in 1 BOTTLE (51270-111-01)
Product Details
What is NDC 51270-111?
What are the uses for Hesol Rim?
Which are Hesol Rim 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)
Which are Hesol Rim 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:
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- BETAINE (UNII: 3SCV180C9W)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LAURETH-23 (UNII: N72LMW566G)
- LAURETH-2 (UNII: D4D38LT1L5)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- URTICA DIOICA (UNII: 710FLW4U46)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MENTHOL (UNII: L7T10EIP3A)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- GINGER OIL (UNII: SAS9Z1SVUK)
* 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".