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Be gone motion sickness tm - Medication Information

Product NDC Code 68428-729
Drug Name

Be gone motion sickness tm

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Increased IgG Production [PE],
Non-Standardized Plant Allergenic Extract [EPC],
Plant Proteins [CS],
Seed Storage Proteins [CS]
Active Ingredients
Anamirta cocculus seed 6 [hp_c]/28g
Kerosene 6 [hp_c]/28g
Strychnos nux-vomica seed 6 [hp_c]/28g
Route ORAL
Dosage Form PELLET
Labeler Name Washington Homeopathic Products
Packages
Package NDC Code Description
68428-729-14 28 g in 1 bottle, plastic (68428-729-14)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENTS COCCULUS 6C NUX VOM 6C PETROLEUM 6C

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
DIRECTIONS Adults 2 pills every 3 hours for 2 days. Then 2 pills morning and night for 2 weeks. Children: 1 pills. Repeat as necessary.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS Sucrose/Lactose

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
INDICATIONS Indications: COCCULUS Motion sickness NUX VOM Vomiting PETROLEUM Nausea

Purpose

Information about the drug product’s indications for use.
USES To relieve the symptoms of traveling sickness from any cause characterized by dizziness, intense nausea, vomiting.

Spl product data elements

Usually a list of ingredients in a drug product.
Be gone Motion Sickness TM ANAMIRTA COCCULUS SEED - STRYCHNOS NUX-VOMICA SEED - KEROSENE SUCROSE LACTOSE ANAMIRTA COCCULUS SEED ANAMIRTA COCCULUS SEED STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED KEROSENE KEROSENE white

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL Be g one TM Motion Sickness label Be g one TM Motion Sickness box image of label image of box

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
KEEP OUT OF REACH OF CHILDREN As with all medications, keep out of reach of children.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
STOP USE AND ASK DOCTOR If symptoms persistor recur, discontinue use. If pregnant or nursing a baby, consult a licensed practitioner before using this product.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API