NDC 50845-0151 Motion Sickness

NDC Product Code 50845-0151

NDC 50845-0151-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Motion Sickness with NDC 50845-0151 is a product labeled by Liddell Laboratories, Inc.. The generic name of Motion Sickness is . The product's dosage form is and is administered via form.

Labeler Name: Liddell Laboratories, Inc.

Dosage Form: -

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.

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)

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
Start Marketing Date: 06-17-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Motion Sickness Product Label Images

Motion Sickness 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:

Cocculus Indicus 200C, Hepar Suis 6X, Nux Vomica 6X, Petroleum 6X, Phosphoricum Acidum 200C, Tabacum 6X.

Indications:

Temporarily relieves symptoms associated with motion sickness (air, car, or sea): dizziness, nausea, vomiting.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Temporarily relieves symptoms associated with motion sickness (air, car, and sea): dizziness, nausea, vomiting.****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 up to each 30 minutes until symptoms are relieved.Children 12 and under:  Consult a doctor prior to use.As a preventative, spray once or twice under the tongue three times per day as needed.

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 51579WWW.LIDDELL.NET  1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELL LABORATORIES37MoSMotion SicknessHOMEOPATHIC1.0 FL. OZ. (30 ml)

* Please review the disclaimer below.