Home FDA labels 2d92fdc4-f628-5432-e063-6394a90a7092 Morning Sickness-Nausea 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 Morning Sickness-Nausea
Generic name CHAMOMILLA, HYDRASTIS CANADENSIS, IRIS VERSICOLOR, BISMUTHUM METALLICUM, BRYONIA, CIMICIFUGA RACEMOSA, GOSSYPIUM HERBACEUM, IPECACUANHA, KREOSOTUM, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, NUX VOMICA, PULSATILLA, SEPIA, SYMPHORICARPUS RACEMOSUS, TABACUM, ZINGIBER OFFICINALE.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9c4a6bf8-5f48-96a8-e053-2a95a90a9757
SPL ID 2d92fdc4-f628-5432-e063-6394a90a7092
Version 2
Effective date 2025-02-07
Source export date 2026-10-12
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:39:27 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Morning Sickness-Nausea openfda.brand_name generic name CHAMOMILLA, HYDRASTIS CANADENSIS, IRIS VERSICOLOR, BISMUTHUM METALLICUM, BRYONIA, CIMICIFUGA RACEMOSA, GOSSYPIUM HERBACEUM, IPECACUANHA, KREOSOTUM, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, NUX VOMICA, PULSATILLA, SEPIA, SYMPHORICARPUS RACEMOSUS, TABACUM, ZINGIBER OFFICINALE. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2483-1 openfda.package_ndc ndc product 55714-2483 openfda.product_ndc ndc11 package 55714248301 derived:openfda.package_ndc spl id 2d92fdc4-f628-5432-e063-6394a90a7092 id spl set id 9c4a6bf8-5f48-96a8-e053-2a95a90a9757 set_id unii 873JZU3ASZ openfda.unii unii 269XH13919 openfda.unii unii QDL83WN8C2 openfda.unii unii 6YR2608RSU openfda.unii unii U015TT5I8H openfda.unii unii 0E53J927NA openfda.unii unii ZW3Z11D0JV openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii 3JYG22FD73 openfda.unii unii VQN1631P4C openfda.unii unii X43D4L3DQC openfda.unii unii G0R4UBI2ZZ openfda.unii unii I76KB35JEV openfda.unii unii C5529G5JPQ openfda.unii unii C88X29Y479 openfda.unii unii K73E24S6X9 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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.