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Gelsemium semp - Medication Information

Product NDC Code 54973-2913
Drug Name

Gelsemium semp

Type Brand
Active Ingredients
Gelsemium sempervirens root 30 [hp_x]/1
Route ORAL
Dosage Form TABLET
Labeler Name Hyland's Inc.
Packages
Package NDC Code Description
54973-2913-4 250 tablet in 1 bottle, plastic (54973-2913-4)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
GELSEMIUM SEMP. 30X

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: Dissolve 4 tablets under tongue 4 times a day. Children: consult a healthcare professional.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Acacia Gum and 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.
DULL HEADACHE & FLU

Purpose

Information about the drug product’s indications for use.
DULL HEADACHE & FLU

Spl product data elements

Usually a list of ingredients in a drug product.
GELSEMIUM SEMP gelsemium sempervirens root ACACIA LACTOSE GELSEMIUM SEMPERVIRENS ROOT GELSEMIUM SEMPERVIRENS ROOT

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 - 250 Tablet Bottle Label SINCE 1903 Hyland's ® HOMEOPATHIC NDC 54973-2913-4 GELSEMIUM SEMP. 30X DULL HEADACHE & FLU* 250 TABLETS *Claims are based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Label

Recent major changes

A list of the section(s) that contain substantive changes that have been approved by FDA in the product labeling. The headings and subheadings, if appropriate, affected by the change are listed together with each section’s identifying number and the month and year on which the change was incorporated in the labeling.
Dosage and Administration (Directions) Adults: Dissolve 4 tablets under tongue 4 times a day. Children: consult a healthcare professional.

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Made according to the Homeopathic Pharmacopoeia of the United States since 1903.

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
If symptoms persist for 7 days or worsen, contact a licensed practitioner.

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if cap band is missing or broken.

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 this and all medicines out of the reach of children.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 800-624-9659

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
To be used according to label indications and/or standard homeopathic indications.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If you are pregnant or nursing, consult a licensed health care professional before using this product.

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.
Warnings Do not use if cap band is missing or broken. If you are pregnant or nursing, consult a licensed health care professional before using this product. If symptoms persist for 7 days or worsen, contact a licensed practitioner. Keep this and all medicines out of the reach of children. To be used according to label indications and/or standard homeopathic indications.

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