NDC 43742-1326 Spinalmax

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

NDC Product Code 43742-1326

NDC Code: 43742-1326

Proprietary Name: Spinalmax 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, Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Picricum Acidum, Silicea, Argentum Metallicum, Calcarea Phosphorica, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum 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

  • 43742 - Deseret Biologicals, Inc.
    • 43742-1326 - Spinalmax

NDC 43742-1326-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Spinalmax with NDC 43742-1326 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Spinalmax is berberis vulgaris, cimicifuga racemosa, cinchona officinalis, colocynthis, ledum palustre, ranunculus bulbosus, aesculus hippocastanum, cuprum aceticum, nadidum, natrum oxalaceticum, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, thiaminum hydrochloricum, alpha-lipoicum acidum, ammonium muriaticum, cartilago suis, discus intervertebralis (suis), picricum acidum, silicea, argentum metallicum, calcarea phosphorica, funiculus umbilicalis suis, glandula suprarenalis suis, gnaphalium polycephalum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

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.

Spinalmax 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
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL
  • RIBOFLAVIN 6 [hp_X]/mL
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • THIOCTIC 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
  • PICRIC ACID 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • SILVER 10 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 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
  • PANTOTHENIC ACID 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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 05-17-2019 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.

Spinalmax Product Label Images

Spinalmax 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 6X, Cuprum Aceticum 6X, Nadidum 6X, Natrum Oxalaceticum 6X, Nicotinamidum 6X, Pyridoxinum Hydrochloricum 6X, Riboflavinum 6X, Thiaminum Hydrochloricum 6X, alpha-Lipoicum Acidum 8X, Ammonium Muriaticum 8X, Cartilago Suis 8X, Discus Intervertebralis (Suis) 8X, Picricum Acidum 8X, Silicea 8X, Argentum Metallicum 10X, Calcarea Phosphorica 10X, Funiculus Umbilicalis Suis 10X, Glandula Suprarenalis Suis 10X, Gnaphalium Polycephalum 10X, Medulla Ossis Suis 10X, Mercurius Praecipitatus Ruber 10X, Pantothenic Acid 10X, Sulphur 28X, Bacillus 7 30C, Gaertner Bacillus (Bach) 30C, Proteus (Morgani) 30C, Proteus (Vulgaris) 30C.

Homeopathic Indications:

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

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

Warnings:

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

Directions:

1-10 drops under the tongue, 3 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:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1326-1HOMEOPATHICSPINALMAX1 FL OZ (30 ml)

* Please review the disclaimer below.

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