Hyaluronic Acid Freeze-dried Powder
NDC 84775-063

View dosage, usage, ingredients, routes, and UNII mappings.
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 UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Hyaluronic Acid Freeze-dried Powder is a OTC MONOGRAPH DRUG-approved product labeled by Shenzhen Fusian Technology Co Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a blue product. This product entry covers the primary NDC 84775-063 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
84775-063
Proprietary Name:
Hyaluronic Acid Freeze-dried Powder
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

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

Marketing Timeline

Start Marketing Date: [9]
11-22-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
I

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. This pharmaceutical product is labeled by Shenzhen Fusian Technology Co Ltd and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 84775-063-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".