NDC 29558-001 Edge
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 29558 - Aloe Vera Industries Pty Ltd
- 29558-001 - Edge
Product Packages
NDC Code 29558-001-01
Package Description: 1 TUBE in 1 CARTON / 7 g in 1 TUBE
Product Details
What is NDC 29558-001?
What are the uses for Edge?
Which are Edge UNII Codes?
The UNII codes for the active ingredients in this product are:
- GAMBIR (UNII: 3NJQ5D8S6N)
- GAMBIR (UNII: 3NJQ5D8S6N) (Active Moiety)
- MUCUNA PRURIENS SEED (UNII: 55G8SQ543S)
- MUCUNA PRURIENS SEED (UNII: 55G8SQ543S) (Active Moiety)
- ERYTHROXYLUM CATUABA BARK (UNII: 3W8LSF0XRN)
- ERYTHROXYLUM CATUABA BARK (UNII: 3W8LSF0XRN) (Active Moiety)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89) (Active Moiety)
- TURNERA DIFFUSA LEAF (UNII: 812R0W1I3K)
- TURNERA DIFFUSA LEAF (UNII: 812R0W1I3K) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- ELEUTHERO (UNII: ZQH6VH092Z)
- ELEUTHERO (UNII: ZQH6VH092Z) (Active Moiety)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U) (Active Moiety)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ) (Active Moiety)
Which are Edge 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)
- JOJOBA OIL (UNII: 724GKU717M)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
* 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".