NDC 54473-337 Exceed Total Care Sensitive Spearmint Tooth Polish
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54473 - Melaleuca, Inc
- 54473-337 - Exceed Total Care Sensitive
Product Characteristics
Product Packages
NDC Code 54473-337-04
Package Description: 93.5 g in 1 TUBE
Product Details
What is NDC 54473-337?
What are the uses for Exceed Total Care Sensitive Spearmint Tooth Polish?
Which are Exceed Total Care Sensitive Spearmint Tooth Polish UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Exceed Total Care Sensitive Spearmint Tooth Polish 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:
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- PROPANEDIOL (UNII: 5965N8W85T)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- XYLITOL (UNII: VCQ006KQ1E)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- ZINC CITRATE (UNII: K72I3DEX9B)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- REBAUDIOSIDE A (UNII: B3FUD0528F)
- SORBITOL (UNII: 506T60A25R)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- 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".