NDC 49741-1019 Medactive Oral Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49741 - Integrate Oral Care, Llc.
- 49741-1019 - Medactive Oral Relief
Product Characteristics
Product Packages
NDC Code 49741-1019-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 49741-1019?
What are the uses for Medactive Oral Relief?
Which are Medactive Oral Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Medactive Oral Relief 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:
- XYLITOL (UNII: VCQ006KQ1E)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETIC ACID (UNII: 9G34HU7RV0)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".