NDC 68703-335 Sciatigon-m

Aconitum Napellus, Berberis Vulgaris, Chamomilla, Colocynthis, Magnesia Phosphorica, Rhus Tox

NDC Product Code 68703-335

NDC Code: 68703-335

Proprietary Name: Sciatigon-m 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.

Non-Proprietary Name: Aconitum Napellus, Berberis Vulgaris, Chamomilla, Colocynthis, Magnesia Phosphorica, Rhus Tox 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.

NDC Code Structure

  • 68703 - Silver Star Brands
    • 68703-335 - Sciatigon-m

NDC 68703-335-02

Package Description: 59 mL in 1 BOTTLE, GLASS

NDC Product Information

Sciatigon-m with NDC 68703-335 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of Sciatigon-m is aconitum napellus, berberis vulgaris, chamomilla, colocynthis, magnesia phosphorica, rhus tox. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Silver Star Brands

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Sciatigon-m Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TOXICODENDRON RADICANS LEAF 30 [hp_C]/59mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]/59mL
  • ACONITUM NAPELLUS 6 [hp_C]/59mL
  • CITRULLUS COLOCYNTHIS FRUIT 30 [hp_C]/59mL
  • BERBERIS VULGARIS FRUIT 6 [hp_X]/59mL
  • MATRICARIA RECUTITA 6 [hp_X]/59mL

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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.

Labeler Name: Silver Star Brands
Labeler Code: 68703
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 07-01-2019 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: 12-31-2020 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: N 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.

Sciatigon-m 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

Hpus Active Ingredients

HPUS Active Ingredients: Equal volumes of each ingredient: Aconitum napellus 6C, Berberis vulgaris 6X, Chamomilla 6X, Colocynthis 30C, Magnesia phosphorica 8X, Rhus tox 30C.The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Uses

Uses: Homeopathic medicine for the temporary relief of sciatic pain and pressure.This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent any disease.

Warnings

Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

For all ages: Mix 0.50 mL in 1/4 cup of water and sip slowly. If preferred, drops may be taken directly in the mouth. Repeat 3-5 times daily. For acute symptoms, repeat every 30 minutes as needed until symptos improve, for up to 48 hours.

Other Safety Information

Contains no artificial flavors or colorants. No gluten added.Tamper resistant for your protection. Use only if safety seal is intact.

Inactive Ingredients

Inactive Ingredients: USP grain alchol (20% by volume), purified water.

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Purpose

Redues occasional pain, pressure & inflammation from sciatica.

* Please review the disclaimer below.

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