NDC 49993-861 Glo Science Antioxidant
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49993-861?
What are the uses for Glo Science Antioxidant?
Which are Glo Science Antioxidant UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Glo Science Antioxidant 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:
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ZINC LACTATE (UNII: 2GXR25858Y)
- FOLIC ACID (UNII: 935E97BOY8)
- CRANBERRY (UNII: 0MVO31Q3QS)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- UBIDECARENONE (UNII: EJ27X76M46)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- GELATIN (UNII: 2G86QN327L)
- ACACIA (UNII: 5C5403N26O)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Glo Science Antioxidant?
- RxCUI: 1046493 - sodium monofluorophosphate 0.84 % Toothpaste
- RxCUI: 1046493 - sodium monofluorophosphate 0.0084 MG/MG Toothpaste
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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".