Home NDC 63083-2075-2 Travel Sickness Drops
Product NDC 63083-2075
Requested package NDC 63083-2075-2
11-digit product format 630832075
Labeler code 63083
Product ID 63083-2075_b63aaff8-bc82-4834-bb1e-c9b2e62e5bf5
Type HUMAN OTC DRUG
Nonproprietary name Travel Sickness Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AETHUSA CYNAPIUM WHOLE; IPECAC; AMBERGRIS; APOMORPHINE HYDROCHLORIDE; ANAMIRTA COCCULUS FRUIT; COLCHICUM AUTUMNALE BULB; LIQUID PETROLEUM; STRYCHNOS NUX-VOMICA SEED; VERATRUM ALBUM ROOT
Active strength 6; 6; 12; 12; 12; 12; 12; 30; 30 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dopamine Agonists [MoA], Dopaminergic Agonist [EPC], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Travel Sickness Drops
Brand name suffix 2075
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AETHUSA CYNAPIUM WHOLE 6 [hp_X]/59mL IPECAC 6 [hp_X]/59mL AMBERGRIS 12 [hp_X]/59mL APOMORPHINE HYDROCHLORIDE 12 [hp_X]/59mL ANAMIRTA COCCULUS FRUIT 12 [hp_X]/59mL COLCHICUM AUTUMNALE BULB 12 [hp_X]/59mL LIQUID PETROLEUM 12 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/59mL VERATRUM ALBUM ROOT 30 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 C75 2026-01-09 C75 2024-01-30 C75 2024-01-30 C75
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2075-2 Travel Sickness Drops2075 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-2075 TRAVEL SICKNESS DROPS 2075 (TRAVEL SICKNESS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_8c9d93bc-a055-458a-8cc0-c984b4b754c0.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-2075-2 63083207502 59 mL in 1 BOTTLE, DROPPER (63083-2075-2) 59 ml 1985-08-15 0000-00-00 No No Current