NDC 83675-031 Joypretty Vitamin C Brightening Eye Serum
Vitamin C Brightening Eye Serum Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83675-031?
What are the uses for Joypretty Vitamin C Brightening Eye Serum?
What are Joypretty Vitamin C Brightening Eye Serum Active Ingredients?
- ASCORBIC ACID 1.5 g/100mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- BUTYLENE GLYCOL 2.68 g/100mL
- DENDROBIUM MONILIFORME WHOLE 1.92 g/100mL
- GLYCERIN 2.5 g/100mL
- HYALURONATE SODIUM .1 g/100mL - A natural high-viscosity mucopolysaccharide with alternating beta (1-3) glucuronide and beta (1-4) glucosaminidic bonds. It is found in the UMBILICAL CORD, in VITREOUS BODY and in SYNOVIAL FLUID. A high urinary level is found in PROGERIA.
- HYDROGENATED STARCH HYDROLYSATE 3.15 g/100mL
- LEONURUS SIBIRICUS LEAF 2 g/100mL
- MALTOOLIGOSYL GLUCOSIDE 3.2 g/100mL
- PROPYLENE GLYCOL 5 g/100mL - A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
- RICE BRAN 2 g/100mL
- SIZOFIRAN 3.2 g/100mL - A beta-D-glucan obtained from the Aphyllophoral fungus Schizophyllum commune. It is used as an immunoadjuvant in the treatment of neoplasms, especially tumors found in the stomach.
- VINCETOXICUM ATRATUM STEM 1.56 g/100mL
Which are Joypretty Vitamin C Brightening Eye Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- MALTOOLIGOSYL GLUCOSIDE (UNII: N91S91EFOG)
- MALTOOLIGOSYL GLUCOSIDE (UNII: N91S91EFOG) (Active Moiety)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- DENDROBIUM MONILIFORME WHOLE (UNII: N7TLA49N8Q)
- DENDROBIUM MONILIFORME WHOLE (UNII: N7TLA49N8Q) (Active Moiety)
- VINCETOXICUM ATRATUM STEM (UNII: 24A2LX7QHE)
- VINCETOXICUM ATRATUM STEM (UNII: 24A2LX7QHE) (Active Moiety)
- SIZOFIRAN (UNII: 7F763NNC9X)
- SIZOFIRAN (UNII: 7F763NNC9X) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
- LEONURUS SIBIRICUS LEAF (UNII: 7U4E311XZK)
- LEONURUS SIBIRICUS LEAF (UNII: 7U4E311XZK) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
- HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)
- HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V) (Active Moiety)
- RICE BRAN (UNII: R60QEP13IC)
- RICE BRAN (UNII: R60QEP13IC) (Active Moiety)
Which are Joypretty Vitamin C Brightening Eye Serum 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:
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROLAMINE (UNII: 9O3K93S3TK)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- WATER (UNII: 059QF0KO0R)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
Which are the Pharmacologic Classes for Joypretty Vitamin C Brightening Eye Serum?
- Allergens - [CS]
- Ascorbic Acid - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Glycerol - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Vitamin C - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".