Home FDA labels a83ef7eb-a246-4123-a21a-529aba6d8bdb Sciatic Nerve Formula 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 Sciatic Nerve Formula
Generic name AESCULUS HIPPOCASTANUM, AMMONIUM MURIATICUM, ARSENICUM ALBUM, BELLADONNA, CAPSICUM ANNUUM, CAUSTICUM, COLCHICUM AUTUMNALE, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, IGNATIA AMARA, KALMIA, MAGNESIA PHOSPHORICA, RHUS TOX AND RUTA GRAVEOLENS.
Manufacturer King Bio Inc.
Product type HUMAN OTC DRUG
SPL set ID 23ca6b5a-c4ca-41df-8dec-323e6e26d534
SPL ID a83ef7eb-a246-4123-a21a-529aba6d8bdb
Version 2
Effective date 2026-03-04
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:01 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Sciatic Nerve Formula openfda.brand_name generic name AESCULUS HIPPOCASTANUM, AMMONIUM MURIATICUM, ARSENICUM ALBUM, BELLADONNA, CAPSICUM ANNUUM, CAUSTICUM, COLCHICUM AUTUMNALE, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, IGNATIA AMARA, KALMIA, MAGNESIA PHOSPHORICA, RHUS TOX AND RUTA GRAVEOLENS. openfda.generic_name manufacturer name King Bio Inc. openfda.manufacturer_name ndc package 57955-9988-2 openfda.package_ndc ndc product 57955-9988 openfda.product_ndc ndc11 package 57955998802 derived:openfda.package_ndc spl id a83ef7eb-a246-4123-a21a-529aba6d8bdb id spl set id 23ca6b5a-c4ca-41df-8dec-323e6e26d534 set_id unii 00UK7646FG openfda.unii unii 01Q9PC255D openfda.unii unii XK4IUX8MNB openfda.unii unii DD5FO1WKFU openfda.unii unii 993QHL78E6 openfda.unii unii 79N6542N18 openfda.unii unii 3C18L6RJAZ openfda.unii unii N94C2U587S openfda.unii unii HF539G9L3Q openfda.unii unii 1NM3M2487K openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii WQZ3G9PF0H openfda.unii unii 36XQ854NWW openfda.unii unii 23H32AOH17 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 Stop use and consult a doctor if symptoms worsen or persist for more than 7 days. If pregnant or breast-feeding, ask a healthcare professional before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.