NDC 53346-1346 Dr. Reckeweg R46 Manurheumin Combination Product
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 53346-1346?
What are the uses for Dr. Reckeweg R46 Manurheumin Combination Product?
Which are Dr. Reckeweg R46 Manurheumin Combination Product UNII Codes?
The UNII codes for the active ingredients in this product are:
- FERRIC PHOSPHATE (UNII: N6BAA189V1)
- FERRIC CATION (UNII: 91O4LML611) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (Active Moiety)
Which are Dr. Reckeweg R46 Manurheumin Combination Product 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:
- ALCOHOL (UNII: 3K9958V90M)
- 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".