NDC 76254-1001 Probee
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76254-1001?
What are the uses for Probee?
Which are Probee UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF) (Active Moiety)
Which are Probee 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- XYLITOL (UNII: VCQ006KQ1E)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MENTHOL (UNII: L7T10EIP3A)
- PEPPERMINT (UNII: V95R5KMY2B)
- MINT (UNII: FV98Z8GITP)
- WATER (UNII: 059QF0KO0R)
* Please review the disclaimer below.
[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".