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  4. NDC Product Code: 80851-301 Vial Kit3.98

NDC 80851-301 Vial Kit3.98

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80851-301?
  4. Vial Kit3.98 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
80851-301
Proprietary Name:
Vial Kit3.98
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oxytical
Labeler Code:
80851
Product Label ID:
b3d0eb54-a3c3-8c7c-e053-2a95a90a946d
Start Marketing Date: [9]
11-11-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 80851-301?

The NDC code 80851-301 is assigned by the FDA to the product Vial Kit3.98 which is product labeled by Oxytical. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80851-301-01 20 ml in 1 bottle, glass . 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 Vial Kit3.98?

[Preparation stage]After cleansing, use toner to clean up the skin.It must be used only after cleansing is complete, and especially pay attention to the cleanliness of your hands.If you use it after exfoliation, you can get more satisfactory results, and it is more effective if you give a simple massage before use.[Application stage]1. Prepare Core peptide(1st), Stable Chitin(2nd) and a syringe.2. Core Peptide(1st) only opens the plastic cap.3. A syringe inlet is injected into the center of the hole at the top of the Core Peptide(1st) to suction. (Total 3ml based on syringe).After the syringe is removed, the inlet is automatically sealed to prevent outside air from entering.4. Open the Stable Chitin(2nd) after referring to the precautions and inject the Core Peptide(1st).Due to the nature of the Stable Chitin component, it is not soluble in ampoule other than Core Peptide. (Not compatible)5. Close the vial opening of the Stable Chitin(2nd) with an elastomer tube and shake to dissolve the Stable Chitin.Check with eyes and if the Stable Chitin component does not appear in the form of a thread (slightly thick), apply it to the skin.

Which are Vial Kit3.98 UNII Codes?

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

  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
  • SAUSSUREA INVOLUCRATA FLOWERING TOP (UNII: 65D06L9K7F)
  • SAUSSUREA INVOLUCRATA FLOWERING TOP (UNII: 65D06L9K7F) (Active Moiety)
  • APIS MELLIFERA VENOM (UNII: 76013O881M)
  • APIS MELLIFERA VENOM (UNII: 76013O881M) (Active Moiety)

Which are Vial Kit3.98 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

[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".