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  4. NDC Product Code: 73303-001 Oliglo Golden Radiance Complete Facial

NDC 73303-001 Oliglo Golden Radiance Complete Facial

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73303-001?
  4. Oliglo Golden Radiance Complete Facial 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.

Get all the details for National Drug Code (NDC) 73303-001 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:
73303-001
Proprietary Name:
Oliglo Golden Radiance Complete Facial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dastmalchi Llc
Labeler Code:
73303
Product Label ID:
08885a8f-fbd4-4412-a0cf-b5f9870f83c0
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
10-30-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 73303-001?

The NDC code 73303-001 is assigned by the FDA to the product Oliglo Golden Radiance Complete Facial which is product labeled by Dastmalchi Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73303-001-01 1 kit in 1 container * 6 ml in 1 package (73303-002-01) * 1 ml in 1 vial (73303-003-01). 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 Oliglo Golden Radiance Complete Facial?

Step 1: Open the Lifting Serum. Align your thumb and index finger around the over your face and neck. You may use lightly under eyes avoding direct contact with eyes, lids, and lips. Leave on for 30 minutes until the mask is completely dry. Step 2: Using lukewarm water, rinse the face and neck until the mask has been removed completely. Setp 3: Open the 24K Gold Hyaluronic Serum. Align your thumb and index finger around the pointy cap. Push backward with light pressure to open. Lightly tap into the palm of your hand to release the serum. Softly massage all over your face and neck, then pat the serum into the skin for a lasting incandescent glow.

Which are Oliglo Golden Radiance Complete Facial UNII Codes?

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

  • BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
  • BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V) (Active Moiety)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0) (Active Moiety)

Which are Oliglo Golden Radiance Complete Facial 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:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".