NDC 63083-2154 Tmj Drops 2154
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2154 - Tmj Drops
Product Packages
NDC Code 63083-2154-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2154?
What are the uses for Tmj Drops 2154?
Which are Tmj Drops 2154 UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ)
- BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE) (UNII: 76TK29UQEZ) (Active Moiety)
- CICUTA VIROSA WHOLE (UNII: 3E698BL84C)
- CICUTA VIROSA WHOLE (UNII: 3E698BL84C) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8)
- BOS TAURUS LIGAMENT (UNII: 0O005HD2J8) (Active Moiety)
- VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172)
- VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA WHOLE (UNII: WYT05213GE) (Active Moiety)
Which are Tmj Drops 2154 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".