FDA.reportPublic FDA data

Nerve Z

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2018-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:49:07

Label at a glance#

ProductNerve Z
Active ingredientMARSDENIA CONDURANGO BARK, ECHINACEA ANGUSTIFOLIA, GINKGO, LIGUSTICUM PORTERI ROOT, MYRRH, PHYTOLACCA AMERICANA ROOT, TABEBUIA IMPETIGINOSA BARK, GOLDENSEAL, PROPOLIS WAX, SUS SCROFA ADRENAL GLAND, SUS SCROFA SPLEEN, SUS SCROFA THYMUS, SUS SCROFA THYROID, GELSEMIUM SEMPERVIRENS ROOT, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, SELENIUM, RANCID BEEF
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

Condurango 3X, Echinacea (Angustifolia) 3X, Ginkgo Biloba 3X, Ligusticum Porteri 3X, Myrrha 3X, Phytolacca Decandra 3X, Tabebuia Impetiginosa 3X, Hydrastis Canadensis 6X, Propolis 6X, Glandula Suprarenalis Suis 8X, Spleen (Suis) 8X, Thymus (Suis) 8X, Thyroidinum (Suis) 8X, Gelsemium Sempervirens 12X, Lycopodium Clavatum 12X, Nux Vomica 12X, Selenium Metallicum 12X, Pyrogenium 30C, 60X, 200X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms of itching, tingling, burning or painful feeling.**

**These statements are based upon traditional 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 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or a 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 of itching, tingling, burning or painful feeling.**

**These statements are based upon traditional 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 43742-0943-1

HOMEOPATHIC

NERVE Z

1 FL OZ (30 ml)

Nerve ZNerve Z

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-094343742-0943-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
MARSDENIA CONDURANGO BARKR23QIR6YBAACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
GINKGO19FUJ2C58TACTIB
LIGUSTICUM PORTERI ROOT81FGO4H42JACTIB
MYRRHJC71GJ1F3LACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
TABEBUIA IMPETIGINOSA BARK6GLA1946WXACTIB
GOLDENSEALZW3Z11D0JVACTIB
PROPOLIS WAX6Y8XYV2NOFACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
SUS SCROFA SPLEEN92AMN5J79YACTIB
SUS SCROFA THYMUS7B69B0BD62ACTIB
SUS SCROFA THYROID6RV024OAUQACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
SELENIUMH6241UJ22BACTIB
RANCID BEEF29SUH5R3HUACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
7a891ecf-7d15-4643-9745-474a3306c06cd65b70f9-e1b3-4916-a1bb-ced2d3c332ef2018-10-01WarningsExact identifier
spl id: 7a891ecf-7d15-4643-9745-474a3306c06c
spl set id: d65b70f9-e1b3-4916-a1bb-ced2d3c332ef

Reported adverse events (FAERS/openFDA)#

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