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Sabina 30c - Medication Information

Product NDC Code 76472-4053
Drug Name

Sabina 30c

Type Brand
Active Ingredients
Juniperus sabina leafy twig 30 [hp_c]/1
Route SUBLINGUAL
Dosage Form PELLET
Labeler Name SEVENE USA
Packages
Package NDC Code Description
76472-4053-1 80 pellet in 1 cylinder (76472-4053-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT HOMEOPATHIC DILUTION OF HPUS SABINA 30C

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/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENT SUCROSE

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.
USE Condition listed above or as directed by a physician.

Purpose

Information about the drug product’s indications for use.
TRADITIONALLY USED FOR: Heavy menstrual flow with pain*

Spl product data elements

Usually a list of ingredients in a drug product.
SABINA 30C SABINA SUCROSE JUNIPERUS SABINA LEAFY TWIG JUNIPERUS SABINA LEAFY TWIG

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.
SABINA 30c P1 SABINA 30c P2 01b lbl

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.
Directions changed.

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 pellet-dispenser seal is 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 out of reach of children.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
OTHER INFORMATION Store at room temperature.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
QUESTIONS? [email protected] * www.ollois.com * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIC DILUTION MAY NOT BE SUSEPTIBLE TO SCIENTIFIC MEASUREMENT.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

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 Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

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

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