NDC 50845-0110 Bladder Uti
Apis Mellifica, Arsenicum Iodatum, Berberis Vulgaris, Cantharis, Coccus Cacti, Echinacea, Mercurius Corrosivus, Rubia Tinctorium, Thuja Occidentalis Liquid Oral

Product Information

Product Code50845-0110
Proprietary Name 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.
Bladder Uti
Non-Proprietary Name 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.
Apis Mellifica, Arsenicum Iodatum, Berberis Vulgaris, Cantharis, Coccus Cacti, Echinacea, Mercurius Corrosivus, Rubia Tinctorium, Thuja Occidentalis
Product Type 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.
Human Otc Drug
Dosage FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
Liddell Laboratories, Inc.
Labeler Code50845
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
11-27-2012
End Marketing Date 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.
03-01-2023
Exclude Flag 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".
N
NDC Code Structure

Usage Information


Product Packages

NDC 50845-0110-2

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

Product Details

Bladder Uti is 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.


What are Bladder Uti Active Ingredients?

The following is the list of active ingredients in 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.


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)


Pharmacologic Class(es)

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.


* Please review the disclaimer below.

Bladder Uti Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



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 sensation
  • frequent need to urinate
  • inflammation
  • painful 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 51579

WWW.LIDDELL.NET

1-800-460-7733


Package Label Display:



ORAL SPRAYS

LIDDELL

LABORATORIES

EST 1994

04  BI+

BLADDER + UTI

(Urinary Tract Infection)

May relieve urinary tract

infection symptoms: burning,

inflammation and frequent

+ painful urination.

HOMEOPATHIC

DOCTOR FORMULATED

Readily absorbed. Safe.

No known side effects. Easy to use.


* Please review the disclaimer below.