NDC 50845-0211 Ear Discomfort

Aconitum Napellus, Anthracinum, Arnica Montana, Baptisa Tinctoria, Capsicum Annuum, Chamomilla, Chenopodium Anthelminticum,

NDC Product Code 50845-0211

NDC CODE: 50845-0211

Proprietary Name: Ear Discomfort 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: Aconitum Napellus, Anthracinum, Arnica Montana, Baptisa Tinctoria, Capsicum Annuum, Chamomilla, Chenopodium Anthelminticum, 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 50845-0211-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Ear Discomfort with NDC 50845-0211 is a a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Ear Discomfort is aconitum napellus, anthracinum, arnica montana, baptisa tinctoria, capsicum annuum, chamomilla, chenopodium anthelminticum, . 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.

Ear Discomfort 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.

  • ACONITUM NAPELLUS 200 [hp_C]/mL
  • BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 200 [hp_C]/mL
  • ARNICA MONTANA 200 [hp_C]/mL
  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • CAPSICUM 6 [hp_X]/mL
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • DYSPHANIA AMBROSIOIDES 6 [hp_X]/mL
  • EUPHORBIA RESINIFERA RESIN 4 [hp_X]/mL
  • LACHESIS MUTA VENOM 200 [hp_C]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]/mL
  • MERCURIC CHLORIDE 200 [hp_C]/mL
  • PLANTAGO MAJOR 3 [hp_X]/mL
  • PULSATILLA VULGARIS 30 [hp_X]/mL
  • VERBASCUM THAPSUS 3 [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: 07-08-2014 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: 06-20-2022 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".

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Ear Discomfort Product Label Images

Ear Discomfort 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

Aconitum Napellus 200C, Anthracinum 200C, Arnica Montana 200C, Baptisia Tinctoria 3X, Capsicum Annuum 6X, Chamomilla 3X, Chenopodium Anthelminticum 6X, Euphorbium Officinarum 4X, Lachesis Mutus 200C, Magnesia Phosphorica 8X, Mercurius Corrosivus 200C, Plantago Major 3X, Pulsatilla (Vulgaris) 30X, Verbascum Thapsus 3X

Indications:

May temporarily relieve symptoms of clogging: pressure, sensitivity, or discomfort of the ear.****These statemetns are based upon traditional homeopathic practice. They have not been reveiwed by the Food and Drug Administration.

May temporarily relieve symptoms of clogging: pressure, sensitivity, or discomfort of the ear.****These statemetns are based upon traditional homeopathic practice. They have not been reveiwed by the Food and Drug Administration.

Warnings:

Stop use and ask a doctor if symptoms persist, there is discharge from the ear, or there is a fever.If pregnant or breast feeding, ask a doctor before use.Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

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.

Directions:

Adults and children over 12: Place 15 drops under the tongue up to six times per day until symptoms are relieved. Children 12 and under: Consult a docotr prior to use.

Inactive Ingredients:

Organic alcohol 20% v/v, Purified water.

Questions:

DIST. BY LIDDELL LABORATORIES INC.WOODBINE, IA 51579WWW.LIDDELL.NET   1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELL LABORATORIES26 ErdEar DiscomfortHOMEOPATHIC1.0 FL. OZ. (30ml)

* Please review the disclaimer below.