NDC 50845-0275 Lung Distress

Product Information

What is NDC 50845-0275?

The NDC code 50845-0275 is assigned by the FDA to the product Lung Distress which is product labeled by Liddell Laboratories. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 50845-0275-2 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0275-1). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code50845-0275
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.		Lung Distress
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Liddell Laboratories
Labeler Code50845
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.		10-05-2021
Listing Expiration Date 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.		12-31-2022
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". 		U
NDC Code Structure

What are the uses for Lung Distress?


Product Packages

NDC Code 50845-0275-2

Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0275-1)

This product is EXCLUDED from the official NDC directory .

Product Details

Lung Distress Active Ingredients UNII Codes

Lung Distress 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.

* Please review the disclaimer below.

Lung Distress Product Label

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.

Product Label Table of Contents



Active Ingredients:



(in each spray) 6.25% of Blatta Orientalis 30C, Bryonia 6X, Carbo Vegetabilis 12X, Eupatorium Perfoliatum 6X, Histaminum Hydrochloricum 200C, Iodium 200C, Ipecacuanha 4X, Lung Suis 6X, Natrum Sulphuricum 30C, Nitricum Acidum 200C, Pulsatilla (Pratensis) 30C, Quebracho 12X, Sambucus Nigra 3X, Sticta Pulmonaria 200C, Urtica Urens 6X, 200C.


Uses:



May temporarily relieve minor symptoms associated with breathing difficulties:

• congestion
• coughing
• wheezing
• tight feeling in the chest**

**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 for more that 3 days, worsen, or if new symptoms occur.

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 health professional before use.

OTHER INFORMATION: Store at room temperature.

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: Spray twice under the tongue 3 times per day. For frequent symptoms, dosage may be taken up to six times the first day.

Children 12 and under: Consult a doctor prior to use.


Indications:



May temporarily relieve minor symptoms associated with breathing difficulties:

• congestion
• coughing
• wheezing
• tight feeling in the chest**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


Inactive Ingredients:



Organic alcohol 20% v/v, Purified water.


Questions:



DIST. BY:

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

16 Lu
Lung Distress

May relieve minor symptoms

associated with breathing

difficulties: congestion, coughing,

wheezing, tight feeling in the chest.

HOMEOPATHIC

DOCTOR FORMULATED

Readily absorbed. Safe.
No known side effects. Easy to use.

1.0 FL OZ. (30 ml)


* Please review the disclaimer below.