NDC 59985-108 Remedi Health Solutions Blistering Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59985-108?
What are the uses for Remedi Health Solutions Blistering Relief Cream?
Which are Remedi Health Solutions Blistering Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- COCOA (UNII: D9108TZ9KG)
- COCOA (UNII: D9108TZ9KG) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
Which are Remedi Health Solutions Blistering Relief Cream 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM CAPROYL LACTYLATE (UNII: 87WR3BHC09)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GUAR GUM (UNII: E89I1637KE)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- LEMON OIL (UNII: I9GRO824LL)
- LIME OIL (UNII: UZH29XGA8G)
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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".