NDC 50845-0155 Caffeine Free
Avena Sativa, Chamomilla, Coffea Cruda, Gratiola Officinalis, Hyoscyamus Niger, Ignatia Amara, Nux Vomica, Paullinia Sorbilis, Thuja Occidentalis, Spray Oral

Product Information

Product Code50845-0155
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.
Caffeine Free
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.
Avena Sativa, Chamomilla, Coffea Cruda, Gratiola Officinalis, Hyoscyamus Niger, Ignatia Amara, Nux Vomica, Paullinia Sorbilis, 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 FormSpray - A liquid minutely divided as by a jet of air or steam.
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.
09-16-2011
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.
09-28-2022
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".
N
NDC Code Structure

Usage Information


Product Packages

NDC 50845-0155-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

Caffeine Free is a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Caffeine Free is avena sativa, chamomilla, coffea cruda, gratiola officinalis, hyoscyamus niger, ignatia amara, nux vomica, paullinia sorbilis, thuja occidentalis, . The product's dosage form is spray and is administered via oral form.


What are Caffeine Free 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.

Caffeine Free 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:



Avena sativa 1X, Chamomilla 3X, Coffea cruda 3X, 200C, Gratiola officinalis 6X, Hyoscyamus niger 200C, Ignatia amara 200C, Nux vomica 200C, Paullinia sorbilis 30X, Thuja occidentalis 6X.


Indications:



May temporarily relieve symptoms associated with caffeine withdrawal: nervousness, headaches, periodic insomnia, and mood changes.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

May temporarily relieve symptoms associated with caffeine withdrawal: nervousness, headaches, periodic insomnia, and mood changes.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.


Warnings:



If symptoms persist, consult a doctor.

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.


Directions:



Adults and children over 12:  Spray twice under the tongue 3 times per day.

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:



DIST. BY  LIDDELL LABORATORIES, INC.

WOODBINE, IA 51579

WWW.LIDDELL.NET1-800-460-7733


Package Label Display:



ORAL SPRAYS
LIDDELL
LABORATORIES


EST. 1994
14 -Inf
Anti-Inflammatory


HOMEOPATHIC


1.0 FL. OZ. (30 ml)


* Please review the disclaimer below.