NDC 73303-001 Oliglo Golden Radiance Complete Facial
Sh-polypeptide-1, Camellia Sinensis Leaf Extract
NDC Product Code 73303-001
NDC Code: 73303-001
Proprietary Name: Oliglo Golden Radiance Complete Facial What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Sh-polypeptide-1, Camellia Sinensis Leaf Extract 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.
NDC Code Structure
- 73303 - Dastmalchi Llc
- 73303-001 - Oliglo Golden Radiance Complete Facial
NDC 73303-001-01
Package Description: 1 KIT in 1 CONTAINER * 6 mL in 1 PACKAGE (73303-002-01) * 1 mL in 1 VIAL (73303-003-01)
NDC Product Information
Oliglo Golden Radiance Complete Facial with NDC 73303-001 is a a human over the counter drug product labeled by Dastmalchi Llc. The generic name of Oliglo Golden Radiance Complete Facial is sh-polypeptide-1, camellia sinensis leaf extract. The product's dosage form is kit and is administered via form.
Dosage Form: Kit - A packaged collection of related material.
Product Type: Human Otc Drug 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.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Dastmalchi Llc
Labeler Code: 73303
Marketing Category: UNAPPROVED DRUG OTHER - 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.
Start Marketing Date: 10-30-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2020 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.
Exclude Flag: N 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
