NDC 72916-112 Schmidts Activated Charcoal With Wondermint Tooth And Mouth
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What is NDC 72916-112?
What are the uses for Schmidts Activated Charcoal With Wondermint Tooth And Mouth?
Which are Schmidts Activated Charcoal With Wondermint Tooth And Mouth 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 Schmidts Activated Charcoal With Wondermint Tooth And Mouth 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)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- XYLITOL (UNII: VCQ006KQ1E)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MAGNOLIA ACUMINATA BARK (UNII: 2U55IJZ60C)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- POMEGRANATE SEED (UNII: 7294Z34NS7)
- COCONUT OIL (UNII: Q9L0O73W7L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- TOCOPHEROL (UNII: R0ZB2556P8)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- TEA TREE OIL (UNII: VIF565UC2G)
- UBIDECARENONE (UNII: EJ27X76M46)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Schmidts Activated Charcoal With Wondermint Tooth And Mouth?
- RxCUI: 1048117 - sodium monofluorophosphate 0.8 % Toothpaste
- RxCUI: 1048117 - sodium monofluorophosphate 0.008 MG/MG Toothpaste
- RxCUI: 1048117 - sodium monofluorophosphate 0.0081 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".