Spinalmax

Manufacturer
Deseret Biologicals, Inc.
Effective date
2016-06-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:25:52

Label at a glance#

ProductSpinalmax
Active ingredientBERBERIS VULGARIS ROOT BARK, BLACK COHOSH, CINCHONA OFFICINALIS BARK, CITRULLUS COLOCYNTHIS FRUIT PULP, LEDUM PALUSTRE TWIG, RANUNCULUS BULBOSUS, HORSE CHESTNUT, CUPRIC ACETATE, NADIDE, SODIUM DIETHYL OXALACETATE, NIACINAMIDE, PICRIC ACID, PYRIDOXINE HYDROCHLORIDE, RIBOFLAVIN, THIAMINE HYDROCHLORIDE, .ALPHA.-LIPOIC ACID, AMMONIUM CHLORIDE, SUS SCROFA CARTILAGE, SUS SCROFA INTERVERTEBRAL DISC, SILICON DIOXIDE, SILVER, TRIBASIC CALCIUM PHOSPHATE, COENZYME A, SUS SCROFA UMBILICAL CORD, SUS SCROFA ADRENAL GLAND, PSEUDOGNAPHALIUM OBTUSIFOLIUM, SUS SCROFA BONE MARROW, MERCURIC OXIDE, SULFUR, ENTEROBACTER CLOACAE, SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS, PROTEUS MORGANII, PROTEUS VULGARIS
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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, 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 30C, Gaertner Bacillus (Bach) 30C, Morgan Bacillus (Pure) 30C, Proteus (Vulgaris) 30C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

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 homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, contact a physician or 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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

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 homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO

NDC 43742-0679-1

HOMEOPATHIC

SPINALMAX

1 FL OZ (30 ml)

SpinalmaxSpinalmax

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 43 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-067943742-0679-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
470e9846-d192-4e1f-a7df-34ef659af623ff83f5d0-7dec-4089-aafe-77e486d9d3352016-06-23WarningsExact identifier
spl id: 470e9846-d192-4e1f-a7df-34ef659af623
spl set id: ff83f5d0-7dec-4089-aafe-77e486d9d335

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.