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NDC 84775-063 Hyaluronic Acid Freeze-dried Powder

Hyaluronic Acid Emulsion Cutaneous - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 84775-063?
  5. Hyaluronic Acid Freeze-dried Powder Uses
  6. Active Ingredients
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 84775-063 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
84775-063
Proprietary Name:
Hyaluronic Acid Freeze-dried Powder
Non-Proprietary Name: [1]
Hyaluronic Acid
Substance Name: [2]
Hyaluronic Acid; Trehalose; Water
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Emulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
Administration Route(s): [4]
Cutaneous - Administration to the skin.
Labeler Name: [5]
Shenzhen Fusian Technology Co Ltd
Labeler Code:
84775
Product Label ID:
277e7049-4fec-f305-e063-6394a90ad873
FDA Application Number: [6]
M016
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
11-22-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)

Code Structure Chart

Product Details

What is NDC 84775-063?

The NDC code 84775-063 is assigned by the FDA to the product Hyaluronic Acid Freeze-dried Powder which is a human over the counter drug product labeled by Shenzhen Fusian Technology Co Ltd. The generic name of Hyaluronic Acid Freeze-dried Powder is hyaluronic acid. The product's dosage form is emulsion and is administered via cutaneous form. The product is distributed in a single package with assigned NDC code 84775-063-01 50 mg in 1 bottle . 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 Hyaluronic Acid Freeze-dried Powder?

Hyaluronic acid freeze-dried powder is a skin care product that mainly replenishes water and repairs, and is widely used to improve a variety of skin problems. The following are its main indications:1. Dehydrated skinSymptoms: The skin is dry, rough, and tight, and even peeling occurs. Functions: Hyaluronic acid freeze-dried powder can deeply replenish water, enhance the skin's moisturizing ability, and relieve dryness symptoms. 2. Damaged skin barrierSymptoms: Skin is sensitive, red, swollen, and easily inflamed, and even tingling occurs, and the barrier function is weakened. Functions: Repair the skin barrier, promote the repair and regeneration of damaged skin, and improve the sensitive state. 3. Early fine lines and dry linesSymptoms: Dry lines and superficial fine lines at the corners of the eyes and mouth caused by water loss. Functions: Replenish skin moisture, improve fine lines caused by dryness, and make the skin look smoother and more elastic. 4. Dull and dull skinSymptoms: The skin is rough, lacks luster, and looks tired. Functions: Improve skin moisture, improve dullness, and restore skin translucency. 5. Skin with acne and acne marks Symptoms: Pigmentation and acne marks are left after acne heals, or the skin's ability to repair is weak. Function: Accelerates acne repair, helps fade acne marks, and promotes skin self-repair. 6. Sensitive skin Symptoms: Strong reaction to external stimuli (such as wind, temperature difference), prone to redness and fever. Function: Calms and soothes the skin, reduces irritation, and enhances skin tolerance. 7. Early aging skin Symptoms: Sagging and dry skin accompanied by loss of collagen, showing signs of aging. Function: Replenishes moisture and locks in moisture, while maintaining skin elasticity and delaying skin aging.

What are Hyaluronic Acid Freeze-dried Powder 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.
  • HYALURONIC ACID 10 mg/50mg - 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.
  • TREHALOSE 10 mg/50mg - An enzyme that catalyzes the conversion of alpha,alpha-trehalose and water to D-glucose. EC 3.2.1.28.
  • WATER 10 mg/50mg - A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)

Which are Hyaluronic Acid Freeze-dried Powder UNII Codes?

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

Which are Hyaluronic Acid Freeze-dried Powder 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".