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  4. NDC Product Code: 83566-117 Melao Rapid Reduction Eye Cream

NDC 83566-117 Melao Rapid Reduction Eye Cream

Limnanthes Alba (meadowfoam) Seed Oil Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83566-117?
  4. Melao Rapid Reduction Eye Cream Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
83566-117
Proprietary Name:
Melao Rapid Reduction Eye Cream
Non-Proprietary Name: [1]
Limnanthes Alba (meadowfoam) Seed Oil
Substance Name: [2]
Agave Tequilana Leaf; Centella Asiatica Root; Chrysanthellum Indicum Flower; Hamamelis Virginiana Top Water; Jojoba Oil; Meadowfoam Seed Oil; Mentha Arvensis Flower Oil; Rosmarinus Officinalis Flower; Saccharum Officinarum Whole
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Guangzhou Yilong Cosmetics Co.,ltd.
    Labeler Code:
    83566
    Product Label ID:
    17d7cafb-fac4-1ed8-e063-6394a90ada7e
    FDA Application Number: [6]
    505G(a)(3)
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    12-20-2023
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83566-117?

    The NDC code 83566-117 is assigned by the FDA to the product Melao Rapid Reduction Eye Cream which is a human over the counter drug product labeled by Guangzhou Yilong Cosmetics Co.,ltd.. The generic name of Melao Rapid Reduction Eye Cream is limnanthes alba (meadowfoam) seed oil. The product's dosage form is cream and is administered via topical form. The product is distributed in a single package with assigned NDC code 83566-117-01 5 g in 1 ampule . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Melao Rapid Reduction Eye Cream?

    This product is used as - Rapidly reduces UNDER-EYE BAGS- Reduces appearance of DARK CIRCLES- Improves PORES- Enhances SKlN texture. 1.Squeeze out pea-size eye cream, and use yourfingertips to apply on the eye bags.2. Pull toward the temple. Don't rub back and forth.3.After applying this product, do not change your facia!expression for 2 minutes.Dependingon individual skin conditions, continue to maintainyour facial expression for 3-8 minutes to solidify the effect

    What are Melao Rapid Reduction Eye Cream Active Ingredients?

    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.

    Which are Melao Rapid Reduction Eye Cream UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
    • MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) (Active Moiety)
    • CHRYSANTHELLUM INDICUM FLOWER (UNII: LG4H57M77Y)
    • CHRYSANTHELLUM INDICUM FLOWER (UNII: LG4H57M77Y) (Active Moiety)
    • MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2)
    • MENTHA ARVENSIS FLOWER OIL (UNII: Q129Z1W6Y2) (Active Moiety)
    • SACCHARUM OFFICINARUM WHOLE (UNII: 3Z20C92XNB)
    • SACCHARUM OFFICINARUM WHOLE (UNII: 3Z20C92XNB) (Active Moiety)
    • ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
    • ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) (Active Moiety)
    • JOJOBA OIL (UNII: 724GKU717M)
    • JOJOBA OIL (UNII: 724GKU717M) (Active Moiety)
    • CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0)
    • CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0) (Active Moiety)
    • AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)
    • AGAVE TEQUILANA LEAF (UNII: 05545M0E3M) (Active Moiety)
    • HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
    • HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) (Active Moiety)

    Which are Melao Rapid Reduction Eye Cream 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:

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    Product Footnotes

    [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".