Cellular Oxygenator Spray
NDC 83027-0118

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 83027-0118?
  4. Cellular Oxygenator Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Cellular Oxygenator (cactus grandiflorus, ascorbicum acidum, nicotinamidum, pyridoxinum hydrochloricum, thiaminum hydrochloricum, magnesium gluconicum dihydricum, riboflavinum, magnesia phosphorica, adenosinum triphosphoricum dinatrum, alpha-lipoicum acidum, anthrachinonum, coenzyme a, nadidum, naja tripudians, ubidecarenonum (coq10)) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nutritional Specialties, Inc.. This medication is typically used as a analogs/derivatives [chemical/ingredient]. It is supplied as a spray for oral administration. This product entry covers the primary NDC 83027-0118 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
83027-0118
Proprietary Name:
Cellular Oxygenator
Non-Proprietary Name: [1]
Cactus Grandiflorus, Ascorbicum Acidum, Nicotinamidum, Pyridoxinum Hydrochloricum, Thiaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Riboflavinum, Magnesia Phosphorica, Adenosinum Triphosphoricum Dinatrum, Alpha-lipoicum Acidum, Anthrachinonum, Coenzyme A, Nadidum, Naja Tripudians, Ubidecarenonum (coq10)
Substance Name: [2]
Adenosine Triphosphate Disodium; Alpha Lipoic Acid; Anthraquinone; Ascorbic Acid; Coenzyme A; Magnesium Gluconate; Magnesium Phosphate, Dibasic Trihydrate; Nadide; Naja Naja Venom; Niacinamide; Pyridoxine Hydrochloride; Riboflavin; Selenicereus Grandiflorus Stem; Thiamine Hydrochloride; Ubidecarenone
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Nutritional Specialties, Inc.
Labeler Code:
83027
Product Label ID:
e5869f25-276f-456a-ab05-2a1899845afb
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-21-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 83027-0118?

The NDC code 83027-0118 is assigned by the FDA to the product Cellular Oxygenator. It is commonly known by its generic name, cactus grandiflorus, ascorbicum acidum, nicotinamidum, pyridoxinum hydrochloricum, thiaminum hydrochloricum, magnesium gluconicum dihydricum, riboflavinum, magnesia phosphorica, adenosinum triphosphoricum dinatrum, alpha-lipoicum acidum, anthrachinonum, coenzyme a, nadidum, naja tripudians, ubidecarenonum (coq10). This pharmaceutical product is labeled by Nutritional Specialties, Inc. and is currently categorized as listed product. The medication is a spray administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 83027-0118-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

What are Active Ingredients of this product?

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.
  • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
  • ALPHA LIPOIC ACID 12 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
  • ANTHRAQUINONE 12 [hp_X]/mL - Compounds based on ANTHRACENES which contain two KETONES in any position. Substitutions can be in any position except on the ketone groups.
  • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • COENZYME A 12 [hp_X]/mL - Venoms from jellyfish; CORALS; SEA ANEMONES; etc. They contain hemo-, cardio-, dermo- , and neuro-toxic substances and probably ENZYMES. They include palytoxin, sarcophine, and anthopleurine.
  • MAGNESIUM GLUCONATE 8 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 10 [hp_X]/mL
  • NADIDE 12 [hp_X]/mL
  • NAJA NAJA VENOM 12 [hp_X]/mL
  • NIACINAMIDE 6 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
  • RIBOFLAVIN 8 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
  • SELENICEREUS GRANDIFLORUS STEM 4 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • UBIDECARENONE 12 [hp_X]/mL

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated 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:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".