NDC 17089-348 Guna-spasm

Atropine Sulfate - Berberis Vulgaris Root Bark - Chelidonium Majus - Cobalt - Cultivated Mushroom - Gelsemium Sempervirens Root - Interleukin-10 - Magnesium - Melatonin - Metenkefalin - Sus Scrofa Sympathetic Nerve - Sus Scrofa Vagus Nerve - Watermelon - Anti-interleukin-1.alpha. Immunoglobulin G Rabbit -

NDC Product Code 17089-348

NDC Code: 17089-348

Proprietary Name: Guna-spasm 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: Atropine Sulfate - Berberis Vulgaris Root Bark - Chelidonium Majus - Cobalt - Cultivated Mushroom - Gelsemium Sempervirens Root - Interleukin-10 - Magnesium - Melatonin - Metenkefalin - Sus Scrofa Sympathetic Nerve - Sus Scrofa Vagus Nerve - Watermelon - Anti-interleukin-1.alpha. Immunoglobulin G Rabbit - 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

  • 17089 - Guna Spa
    • 17089-348 - Guna-spasm

NDC 17089-348-18

Package Description: 1 BOTTLE, DROPPER in 1 BOX > 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Guna-spasm with NDC 17089-348 is a a human over the counter drug product labeled by Guna Spa. The generic name of Guna-spasm is atropine sulfate - berberis vulgaris root bark - chelidonium majus - cobalt - cultivated mushroom - gelsemium sempervirens root - interleukin-10 - magnesium - melatonin - metenkefalin - sus scrofa sympathetic nerve - sus scrofa vagus nerve - watermelon - anti-interleukin-1.alpha. immunoglobulin g rabbit -. The product's dosage form is solution/ drops and is administered via oral form.

Labeler Name: Guna Spa

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

Guna-spasm 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.

  • CULTIVATED MUSHROOM 4 [hp_X]/30mL
  • ANTI-INTERLEUKIN-1.ALPHA. IMMUNOGLOBULIN G RABBIT 4 [hp_C]/30mL
  • ATROPINE SULFATE 6 [hp_X]/30mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/30mL
  • METENKEFALIN 4 [hp_C]/30mL
  • CHELIDONIUM MAJUS 4 [hp_X]/30mL
  • COBALT 4 [hp_X]/30mL
  • WATERMELON 4 [hp_X]/30mL
  • GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/30mL
  • INTERLEUKIN-10 4 [hp_C]/30mL
  • MAGNESIUM 4 [hp_X]/30mL
  • MELATONIN 4 [hp_C]/30mL
  • SUS SCROFA SYMPATHETIC NERVE 200 [hp_X]/30mL
  • SUS SCROFA VAGUS NERVE 6 [hp_X]/30mL

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)

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: Guna Spa
Labeler Code: 17089
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: 04-16-2008 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.

Guna-spasm Product Label Images

Guna-spasm 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/Purpose

AGARICUS CAMPESTRIS         4X    ANTISPASTICANTI INTERLEUKIN 1 ALPHA      4C    ANTI-INFLAMMATORYATROPINUM SULFURICUM         6X    PAIN RELIEFBERBERIS VULGARIS         3X    DETOXIFICATIONBETA-ENDORPHIN             4C    PAIN RELIEFCHELIDONIUM MAJUS         4X    DETOXIFICATIONCOBALTUM METALLICUM         4X    ANTISPASTIC COLOCYNTHIS             4X    BACK SOREGELSEMIUM              6X     ANALGESICINTERLEUKIN 10             4C    ANTI-INFLAMMATORYMAGNESIUM METALLICUM         4X    ANTISPASTICMELATONIN             4C    ANTISPASTICSYMPATHETIC NERVE        200X    PAIN RELIEFVAGAL NERVE            6X    PAIN RELIEF

Uses

For the temporary relief of symptoms of minor musculoskeletal pain due to Spasm and Hypertonic Muscles

Warnings

Stop use and ask doctor if symptoms of spasms worsen or persist more than 5 days

Keep this and all medicines out of reach of  children

Pregnancy

If pregnant or breast-feeding ask a doctor before use

Directions

Take 15 minutes before mealsAdults and children 12 years and older    20 drops in a little, 2 times per dayChildren  between 12 years and 6 years of age    10 drops in a little water, 2 times per dayChildren under 6 years     5 drops in a glass of water, 2 times per day

Questions

Questions?: info@gunainc.com, tel. (484) 223-3500

* Please review the disclaimer below.

Previous Code
17089-347
Next Code
17089-349