NDC 58368-006 Neorelief Wound Care
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 58368-006?
What are the uses for Neorelief Wound Care?
Which are Neorelief Wound Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
- STELLARIA MEDIA (UNII: 2H03479QVR)
- STELLARIA MEDIA (UNII: 2H03479QVR) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (Active Moiety)
Which are Neorelief Wound Care 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:
- METHYL GLUCOSE DIOLEATE (UNII: FA9KFJ4Z6P)
- WATER (UNII: 059QF0KO0R)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- SILVER (UNII: 3M4G523W1G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CLOVE OIL (UNII: 578389D6D0)
- EMU OIL (UNII: 344821WD61)
- HYALURONIC ACID (UNII: S270N0TRQY)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
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[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".