Home FDA labels 7074e857-cf0c-4e2f-aac5-f9df8f4d614a Nerve Z openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Nerve Z
Generic name CONDURANGO, ECHINACEA (ANGUSTIFOLIA), GINKGO BILOBA, LIGUSTICUM PORTERI, MYRRHA, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, PROPOLIS, GLANDULA SUPRARENALIS SUIS, SPLEEN (SUIS), TABEBUIA IMPETIGINOSA, THYMUS (SUIS), THYROIDINUM (SUIS), GELSEMIUM SEMPERVIRENS, LYCOPODIUM CLAVATUM, NUX VOMICA, SELENIUM METALLICUM, PYROGENIUM
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 4e4c1cb3-d5cc-4183-b9fc-ccdc7275dbaa
SPL ID 7074e857-cf0c-4e2f-aac5-f9df8f4d614a
Version 4
Effective date 2024-08-20
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:15 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Nerve Z openfda.brand_name generic name CONDURANGO, ECHINACEA (ANGUSTIFOLIA), GINKGO BILOBA, LIGUSTICUM PORTERI, MYRRHA, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, PROPOLIS, GLANDULA SUPRARENALIS SUIS, SPLEEN (SUIS), TABEBUIA IMPETIGINOSA, THYMUS (SUIS), THYROIDINUM (SUIS), GELSEMIUM SEMPERVIRENS, LYCOPODIUM CLAVATUM, NUX VOMICA, SELENIUM METALLICUM, PYROGENIUM openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1315-1 openfda.package_ndc ndc product 43742-1315 openfda.product_ndc ndc11 package 43742131501 derived:openfda.package_ndc spl id 7074e857-cf0c-4e2f-aac5-f9df8f4d614a id spl set id 4e4c1cb3-d5cc-4183-b9fc-ccdc7275dbaa set_id unii 6RV024OAUQ openfda.unii unii 11E6VI8VEG openfda.unii unii 269XH13919 openfda.unii unii 639KR60Q1Q openfda.unii unii 29SUH5R3HU openfda.unii unii VB06AV5US8 openfda.unii unii 92AMN5J79Y openfda.unii unii 6Y8XYV2NOF openfda.unii unii ZW3Z11D0JV openfda.unii unii 398IYQ16YV openfda.unii unii 19FUJ2C58T openfda.unii unii 81FGO4H42J openfda.unii unii 6GLA1946WX openfda.unii unii C88X29Y479 openfda.unii unii H6241UJ22B openfda.unii unii JC71GJ1F3L openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.