NDC 61941-0132 Organix Complete
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61941-0132?
What are the uses for Organix Complete?
Which are Organix Complete UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- PECTIN (UNII: 89NA02M4RX)
- PECTIN (UNII: 89NA02M4RX) (Active Moiety)
Which are Organix Complete 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:
- THYME (UNII: CW657OBU4N)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- SUCROSE (UNII: C151H8M554)
- SAGE (UNII: 065C5D077J)
- ELM (UNII: 63POE2M46Y)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYSSOP (UNII: X7HKN4FOJI)
- PEPPERMINT OIL (UNII: AV092KU4JH)
What is the NDC to RxNorm Crosswalk for Organix Complete?
- RxCUI: 1111086 - Organix Complete 2.5 MG / 1.7 MG Oral Lozenge
- RxCUI: 1111086 - menthol 2.5 MG / pectin 1.7 MG Oral Lozenge [Organix Complete]
- RxCUI: 1111086 - Organix Complete (menthol 2.5 MG / pectin 1.7 MG) Oral Lozenge
- RxCUI: 749244 - menthol 2.5 MG / pectin 1.7 MG Oral Lozenge
* 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".