NDC 63083-2038 Small Joint Pain Drops 2038
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2038?
What are the uses for Small Joint Pain Drops 2038?
Which are Small Joint Pain Drops 2038 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U)
- RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ) (Active Moiety)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (Active Moiety)
- AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB) (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)
Which are Small Joint Pain Drops 2038 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)
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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".