Home FDA labels 2779f075-075c-413a-b4a9-e8e0f4c2d586 MOTION SICKNESS HP 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 MOTION SICKNESS HP
Generic name ARNICA MONTANA, BRYONIA ALBA ROOT, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS IGNATII SEED, IPECAC, POTASSIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, VERATRUM ALBUM ROOT
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID 61da7048-b9a9-4af1-b1fc-c30dbaa66f1b
SPL ID 2779f075-075c-413a-b4a9-e8e0f4c2d586
Version 2
Effective date 2023-01-03
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:31 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name MOTION SICKNESS HP openfda.brand_name generic name ARNICA MONTANA, BRYONIA ALBA ROOT, QUININE SULFATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, STRYCHNOS IGNATII SEED, IPECAC, POTASSIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, SEPIA OFFICINALIS JUICE, TOBACCO LEAF, VERATRUM ALBUM ROOT openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0099-1 openfda.package_ndc ndc product 43406-0099 openfda.product_ndc ndc11 package 43406009901 derived:openfda.package_ndc spl id 2779f075-075c-413a-b4a9-e8e0f4c2d586 id spl set id 61da7048-b9a9-4af1-b1fc-c30dbaa66f1b set_id unii 269XH13919 openfda.unii unii O80TY208ZW openfda.unii unii Q28R5GF371 openfda.unii unii QDL83WN8C2 openfda.unii unii 6YR2608RSU openfda.unii unii 1NM3M2487K openfda.unii unii BQN1B9B9HA openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii 810258W28U openfda.unii unii QNS6W5US1Z openfda.unii unii KF7Z0E0Q2B 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 WARNING: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN . In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use it TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.