NDC 59985-113 Remedi Health Solutions Spider Bite Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59985-113?
What are the uses for Remedi Health Solutions Spider Bite Cream?
Which are Remedi Health Solutions Spider Bite Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBO ANIMALIS (UNII: 279O8I0433)
- CARBO ANIMALIS (UNII: 279O8I0433) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2)
- LOXOSCELES RECLUSA (UNII: 039G4OZ3G2) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
Which are Remedi Health Solutions Spider Bite 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".