NDC 73303-001 Oliglo Golden Radiance Complete Facial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73303 - Dastmalchi Llc
- 73303-001 - Oliglo Golden Radiance Complete Facial
Product Packages
NDC Code 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)
Product Details
What is NDC 73303-001?
What are the uses for Oliglo Golden Radiance Complete Facial?
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:
- WATER (UNII: 059QF0KO0R)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)
- CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0)
- CHAMOMILE (UNII: FGL3685T2X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
- LILIUM CANDIDUM BULB (UNII: AHG15J8AM0)
- NARCISSUS PSEUDONARCISSUS FLOWER (UNII: L879RBF1WN)
- LEONTOPODIUM NIVALE SUBSP. ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
- POLYEPSILON-LYSINE (4000 MW) (UNII: WB0M8X4TWR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCINE (UNII: TE7660XO1C)
- SERINE (UNII: 452VLY9402)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
- LEUCINE (UNII: GMW67QNF9C)
- ALANINE (UNII: OF5P57N2ZX)
* Please review the disclaimer below.
[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".