NDC 63083-6027 Spa/pool Detox 6027
Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 63083-6027 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 63083-6027?
What are the uses for Spa/pool Detox 6027?
What are Spa/pool Detox 6027 Active Ingredients?
- AMMONIUM CATION 30 [hp_X]/59mL
- BROMINE 30 [hp_X]/59mL - A halogen with the atomic symbol Br, atomic number 35, and atomic weight 79.904. It is a volatile reddish-brown liquid that gives off suffocating vapors, is corrosive to the skin, and may cause severe gastroenteritis if ingested.
- CHLORINE 12 [hp_X]/59mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
- CRYPTOSPORIDIUM HOMINIS 30 [hp_X]/59mL
- CUPRIC CATION 30 [hp_X]/59mL
- ESCHERICHIA COLI 30 [hp_X]/59mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
- ETIDRONIC ACID 30 [hp_X]/59mL - A diphosphonate which affects calcium metabolism. It inhibits ectopic calcification and slows down bone resorption and bone turnover.
- SODIUM CARBONATE 12 [hp_X]/59mL
- SODIUM CATION 30 [hp_X]/59mL
Which are Spa/pool Detox 6027 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CARBONATE (UNII: 45P3261C7T)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- CUPRIC CATION (UNII: 8CBV67279L)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- AMMONIUM CATION (UNII: 54S68520I4)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- SODIUM CATION (UNII: LYR4M0NH37)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- ETIDRONIC ACID (UNII: M2F465ROXU)
- ETIDRONIC ACID (UNII: M2F465ROXU) (Active Moiety)
- CRYPTOSPORIDIUM HOMINIS (UNII: DKE8M34J72)
- CRYPTOSPORIDIUM HOMINIS (UNII: DKE8M34J72) (Active Moiety)
- ESCHERICHIA COLI (UNII: 514B9K0L10)
- ESCHERICHIA COLI (UNII: 514B9K0L10) (Active Moiety)
Which are Spa/pool Detox 6027 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)
Which are the Pharmacologic Classes for Spa/pool Detox 6027?
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Bisphosphonate - [EPC] (Established Pharmacologic Class)
- Diphosphonates - [CS]
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
* 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, 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".