NDC 49726-040 Respitrol
Ammonium Carbonicum,Antimonium Tartaricum,Bromium,Carbo Vegetabilis,Chlorinum,Kali - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49726 - Hellolife, Inc.
- 49726-040 - Respitrol
Product Characteristics
Product Packages
NDC Code 49726-040-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 49726-040?
What are the uses for Respitrol?
What are Respitrol Active Ingredients?
- ACTIVATED CHARCOAL 10 [hp_X]/1
- AMMONIUM CARBONATE 10 [hp_X]/1
- ANTIMONY POTASSIUM TARTRATE 10 [hp_X]/1 - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- BROMINE 10 [hp_X]/1 - 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 10 [hp_X]/1 - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
- LOBELIA INFLATA 10 [hp_X]/1 - A plant genus of the family CAMPANULACEAE used medicinally and is a source of LOBELINE.
- POTASSIUM CARBONATE 10 [hp_X]/1
- SULFURIC ACID 10 [hp_X]/1
- TIN 10 [hp_X]/1 - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
Which are Respitrol UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
Which are Respitrol 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:
- SORBITOL (UNII: 506T60A25R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 2S7830E561)
- COPOVIDONE (UNII: D9C330MD8B)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
* 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".