NDC 63083-1016 Trees 1 1016
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 63083-1016 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 63083-1016?
What are the uses for Trees 1 1016?
Which are Trees 1 1016 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- ALNUS RHOMBIFOLIA BARK (UNII: 0FIE1UZN3V)
- ALNUS RHOMBIFOLIA BARK (UNII: 0FIE1UZN3V) (Active Moiety)
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557)
- FRAXINUS LATIFOLIA WHOLE (UNII: 024W88F557) (Active Moiety)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976)
- BETULA OCCIDENTALIS POLLEN (UNII: R889N2L976) (Active Moiety)
- JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY)
- JUNIPERUS SCOPULORUM POLLEN (UNII: 0G82TT8ZFY) (Active Moiety)
- POPULUS TRICHOCARPA WHOLE (UNII: 19Q34QZ03Z)
- POPULUS TRICHOCARPA WHOLE (UNII: 19Q34QZ03Z) (Active Moiety)
- HESPEROCYPARIS ARIZONICA POLLEN (UNII: 232DMH0XVF)
- HESPEROCYPARIS ARIZONICA POLLEN (UNII: 232DMH0XVF) (Active Moiety)
- ELM (UNII: 63POE2M46Y)
- ELM (UNII: 63POE2M46Y) (Active Moiety)
- ABIES BALSAMEA LEAF OIL (UNII: 2FGT9T2SQC)
- ABIES BALSAMEA LEAF OIL (UNII: 2FGT9T2SQC) (Active Moiety)
- PSEUDOTSUGA MENZIESII RESIN (UNII: 8N34F5Z76Y)
- PSEUDOTSUGA MENZIESII RESIN (UNII: 8N34F5Z76Y) (Active Moiety)
- CARYA LACINIOSA BARK (UNII: 98Q86P6WFR)
- CARYA LACINIOSA BARK (UNII: 98Q86P6WFR) (Active Moiety)
- ACER PENSYLVANICUM WHOLE (UNII: 01B3X858LI)
- ACER PENSYLVANICUM WHOLE (UNII: 01B3X858LI) (Active Moiety)
- WHITE MULBERRY (UNII: MN25R0HH5A)
- WHITE MULBERRY (UNII: MN25R0HH5A) (Active Moiety)
- QUERCUS LOBATA POLLEN (UNII: HGH5K3653K)
- QUERCUS LOBATA POLLEN (UNII: HGH5K3653K) (Active Moiety)
- QUERCUS VELUTINA POLLEN (UNII: 294L626TT0)
- QUERCUS VELUTINA POLLEN (UNII: 294L626TT0) (Active Moiety)
- PINUS STROBUS CONE (UNII: K39FUU78ES)
- PINUS STROBUS CONE (UNII: K39FUU78ES) (Active Moiety)
- BIANCAEA SAPPAN WOOD (UNII: 086263LQDD)
- BIANCAEA SAPPAN WOOD (UNII: 086263LQDD) (Active Moiety)
- PICEA PUNGENS POLLEN (UNII: R9JBC6687X)
- PICEA PUNGENS POLLEN (UNII: R9JBC6687X) (Active Moiety)
Which are Trees 1 1016 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.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".