NDC 75053-0003 Celltem
Carbo Vegetabilis,Anilinum,Radium Bromatum,Millefolium,Medulla Ossis - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75053 - Nucleic Products, Llc
- 75053-0003 - Celltem
Product Packages
NDC Code 75053-0003-1
Package Description: 118 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 75053-0003?
What are the uses for Celltem?
What are Celltem Active Ingredients?
- ACHILLEA MILLEFOLIUM WHOLE 13 [hp_X]/mL
- ACTIVATED CHARCOAL 9 [hp_X]/mL
- ANILINE 9 [hp_X]/mL
- ARTEMISIA ABROTANUM FLOWERING TOP 200 [hp_C]/mL
- CALCIUM OXALATE MONOHYDRATE 200 [hp_C]/mL - The calcium salt of oxalic acid, occurring in the urine as crystals and in certain calculi.
- CONIUM MACULATUM FLOWERING TOP 200 [hp_C]/mL
- EUPHORBIA COROLLATA ROOT 200 [hp_C]/mL
- EUPHORBIA RESINIFERA RESIN 200 [hp_C]/mL
- HERRING SPERM DNA 6 [hp_C]/mL
- METHYLENE BLUE 9 [hp_C]/mL - A compound consisting of dark green crystals or crystalline powder, having a bronze-like luster. Solutions in water or alcohol have a deep blue color. Methylene blue is used as a bacteriologic stain and as an indicator. It inhibits GUANYLATE CYCLASE, and has been used to treat cyanide poisoning and to lower levels of METHEMOGLOBIN.
- RADIUM BROMIDE 12 [hp_X]/mL
- SACCHAROMYCES CEREVISIAE RNA 5 [hp_C]/mL
- SUS SCROFA BONE MARROW 3 [hp_C]/mL
Which are Celltem UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- ANILINE (UNII: SIR7XX2F1K)
- ANILINE (UNII: SIR7XX2F1K) (Active Moiety)
- RADIUM BROMIDE (UNII: R74O7T8569)
- RADIUM CATION (UNII: 05456MVL7T) (Active Moiety)
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- HERRING SPERM DNA (UNII: 51FI676N6F)
- HERRING SPERM DNA (UNII: 51FI676N6F) (Active Moiety)
- METHYLENE BLUE (UNII: T42P99266K)
- METHYLENE BLUE CATION (UNII: ZMZ79891ZH) (Active Moiety)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0)
- ARTEMISIA ABROTANUM FLOWERING TOP (UNII: QG07G580U0) (Active Moiety)
- CALCIUM OXALATE MONOHYDRATE (UNII: 4PP86KK527)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- EUPHORBIA COROLLATA ROOT (UNII: Z1UW424Q9Z)
- EUPHORBIA COROLLATA ROOT (UNII: Z1UW424Q9Z) (Active Moiety)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K)
- EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (Active Moiety)
Which are Celltem 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Celltem?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Oxidation-Reduction Activity - [MoA] (Mechanism of Action)
- Oxidation-Reduction Agent - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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 ("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".