NDC 50845-0110 Bladder Uti

Apis Mellifica, Arsenicum Iodatum, Berberis Vulgaris, Cantharis, Coccus Cacti, Echinacea, Mercurius Corrosivus, Rubia Tinctorium, Thuja Occidentalis

NDC Product Code 50845-0110

NDC CODE: 50845-0110

Proprietary Name: Bladder Uti What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Apis Mellifica, Arsenicum Iodatum, Berberis Vulgaris, Cantharis, Coccus Cacti, Echinacea, Mercurius Corrosivus, Rubia Tinctorium, Thuja Occidentalis 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.

NDC Code Structure

  • 50845 - Liddell Laboratories, Inc.

NDC 50845-0110-2

Package Description: 1 BOTTLE, SPRAY in 1 CARTON > 30 mL in 1 BOTTLE, SPRAY (50845-0110-1)

NDC Product Information

Bladder Uti with NDC 50845-0110 is a a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Bladder Uti is apis mellifica, arsenicum iodatum, berberis vulgaris, cantharis, coccus cacti, echinacea, mercurius corrosivus, rubia tinctorium, thuja occidentalis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Liddell Laboratories, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Bladder Uti Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • APIS MELLIFERA 200 [hp_C]/mL
  • ARSENIC TRIIODIDE 200 [hp_C]/mL
  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
  • LYTTA VESICATORIA 200 [hp_C]/mL
  • PROTORTONIA CACTI 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
  • MERCURIC CHLORIDE 200 [hp_C]/mL
  • RUBIA TINCTORUM ROOT 1 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAF 200 [hp_C]/mL
  • GINGER 6 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Liddell Laboratories, Inc.
Labeler Code: 50845
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 11-27-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 03-01-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Bladder Uti Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Apis Mellifica 200C, Arsenicum Iodatum 200C, Berberis Vulgaris 6X, Cantharis 200C, Coccus Cacti 3X, Echinacea 1X, Mercurius Corrosivus 200C, Rubia Tinctorum 1X, Thuja Occidentalis 200C, Zingiber Officinale 6X.

Indications:

  • May temporarily relieve these symptoms associated with urinary tract infections:burning sensationfrequent need to urinateinflammationpainful urination****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve these symptoms associated with urinary tract infections:•  burning sensation•  frequent need to urinate•  inflammation•  painful urination****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings:

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.Stop use and ask a doctor if symptoms persist, are severe, or you experience fever, chills, back pain or bloody urine. You may have a serious condition that requires professional treatment.Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.If pregnant or breast feeding, ask a doctor before using product.Do not use if Tamper Evident seal around neck of bottle is missing or broken.Store at room temperature.

Directions:

Adults and children over 12 Spray twice under the tongue three times per day. For severe symptoms, dosage may be taken up to six times the first day. Continue dosage for fourteen days after symptoms have subsided. Children 12 and under Consult a doctor prior to use.

Inactive Ingredients:

Organic alcohol 20% v/v, Purified Water.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

Questions:

LIDDELL LABORATORIES INC.201 APPLE BLVD.WOODBINE, IA 51579WWW.LIDDELL.NET1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELLLABORATORIESEST 199404  BI+BLADDER + UTI(Urinary Tract Infection)May relieve urinary tractinfection symptoms: burning,inflammation and frequent+ painful urination.HOMEOPATHICDOCTOR FORMULATEDReadily absorbed. Safe.No known side effects. Easy to use.

* Please review the disclaimer below.