NDC 70417-002 Olea Olidental
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What is NDC 70417-002?
What are the uses for Olea Olidental?
Which are Olea Olidental UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Olea Olidental 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:
- ALCLOXA (UNII: 18B8O9DQA2)
- AMINOCAPROIC ACID (UNII: U6F3787206)
- CHAMOMILE (UNII: FGL3685T2X)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- CLARY SAGE (UNII: U3HSK5JC0Q)
- ALOE (UNII: V5VD430YW9)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- XYLITOL (UNII: VCQ006KQ1E)
- GLUCOSYL STEVIOL (UNII: TKD5UC898Q)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
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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".