NDC 62185-0016 Ns Support

Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis,

NDC Product Code 62185-0016

NDC CODE: 62185-0016

Proprietary Name: Ns Support 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: Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Niacinamide (nicotinamide) is a form of vitamin B3 (niacin) and is used to prevent and treat niacin deficiency (pellagra). Niacin deficiency can cause diarrhea, confusion (dementia), tongue redness/swelling, and peeling red skin. Niacinamide is often used instead of niacin because it causes fewer side effects (e.g., flushing). Unlike niacin, niacinamide does not help correct blood fat levels and cannot be substituted for niacin if you are being treated for a blood fat problem (e.g., high cholesterol). Niacin deficiency may happen as a result of poor diet, certain medical conditions (e.g., alcohol abuse, malabsorption syndrome, Hartnup disease), or long-term use of certain medications (e.g., isoniazid). It is best to get your vitamins from healthy foods. A multivitamin may be recommended by your doctor instead of niacinamide because poor diet usually causes deficiencies in more than one vitamin. Vitamins help to support the body's ability to make and break down natural substances (metabolism) and are needed for good health.

NDC Code Structure

  • 62185 - Dr. Donna Restivo Dc

NDC 62185-0016-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Ns Support with NDC 62185-0016 is a a human over the counter drug product labeled by Dr. Donna Restivo Dc. The generic name of Ns Support is berberis vulgaris, cimicifuga racemosa, cinchona officinalis, colocynthis, ledum palustre, ranunculus bulbosus, aesculus hippocastanum, cuprum aceticum, nadidum, natrum oxalaceticum, nicotinamidum, picricum acidum, pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, alpha-lipoicum acidum, ammonium muriaticum, cartilago suis, discus intervertebralis (suis), silicea, argentum metallicum, calcarea phosphorica, coenzyme a, funiculus umbilicalis suis, glandula suprarenalis suis, . The product's dosage form is liquid and is administered via oral form.

Labeler Name: Dr. Donna Restivo Dc

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.

Ns Support 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.

  • BERBERIS VULGARIS ROOT BARK 4 [hp_X]/mL
  • BLACK COHOSH 4 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 4 [hp_X]/mL
  • CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X]/mL
  • LEDUM PALUSTRE TWIG 4 [hp_X]/mL
  • RANUNCULUS BULBOSUS 4 [hp_X]/mL
  • HORSE CHESTNUT 6 [hp_X]/mL
  • CUPRIC ACETATE 6 [hp_X]/mL
  • NADIDE 6 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
  • NIACINAMIDE 6 [hp_X]/mL
  • PICRIC ACID 6 [hp_X]/mL
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL
  • RIBOFLAVIN 6 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/mL
  • AMMONIUM CHLORIDE 8 [hp_X]/mL
  • SUS SCROFA CARTILAGE 8 [hp_X]/mL
  • SUS SCROFA INTERVERTEBRAL DISC 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • SILVER 10 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 10 [hp_X]/mL
  • COENZYME A 10 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 10 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 10 [hp_X]/mL
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM 10 [hp_X]/mL
  • SUS SCROFA BONE MARROW 10 [hp_X]/mL
  • MERCURIC OXIDE 10 [hp_X]/mL
  • SULFUR 28 [hp_X]/mL
  • ENTEROBACTER CLOACAE 30 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL
  • PROTEUS VULGARIS 30 [hp_C]/mL

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.

  • WATER (UNII: 059QF0KO0R)
  • 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.
  • 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: Dr. Donna Restivo Dc
Labeler Code: 62185
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: 03-02-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 10-14-2020 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Ns Support Product Label Images

Ns Support 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:

Berberis Vulgaris 4X, Cimicifuga Racemosa 4X, Cinchona Officinalis 4X, Colocynthis 4X, Ledum Palustre 4X, Ranunculus Bulbosus 4X, Aesculus Hippocastanum 4X, Cuprum Aceticum 6X, Nadidum 6X, Natrum Oxalaceticum 6X, Nicotinamidum 6X, Picricum Acidum 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Thiaminum Hydrochloricum 6X, Alpha Lipoicum Acidum 8X, Ammonium Muriaticum 8X, Cartilago Suis 8X, Discus Intervertebralis (suis) 8X, Silicea 8X, Argentum Metallicum 10X, Calcarea Phosphorica 10X, Coenzyme A 10X, Funiculus Umbilicalis Suis 10X, Glandula Suprarenalis Suis 10X, Gnaphalium Polycephalum 10X, Medulla Ossis Suis 10X, Mercurius Praecipitatus Ruber 10X, Sulphur 28X, Bacillus 7 (Enterobacter Cloacae) 30C, Gaertner Bacillus (Bach) 30C, Morgan Bacillus (pure) 30C, Proteus (Vulgaris) 30C.

Homeopathic Indications:

For temporary relief of symptoms related to a blocked spine including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to a blocked spine including spasm, pain, anxiety, nervousness and the inability to hold chiropractic spinal adjustments.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: Sealed for your protection.Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops under the tongue, 3 to 6 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 25% ethanol

Questions:

Distributed by Dr. Donna Restivo DC, Wellness Consultant822 South Lake Blvd. Mahopac, New York 10541www.mahopacmassage.com • (845) 628-6286

Package Label Display:

DR. DONNA RESTIVO DCWELLNESS CONSULTANTNDC 62185-0016-1HOMEOPATHICNS SUPPORT1 FL OZ (30 ml)

* Please review the disclaimer below.