Home NDC 63083-2115-2 Vertigo Syncope Drops
Product NDC 63083-2115
Requested package NDC 63083-2115-2
11-digit product format 630832115
Labeler code 63083
Product ID 63083-2115_a714711b-afd8-4407-81e6-e9cc56420a66
Type HUMAN OTC DRUG
Nonproprietary name Vertigo Syncope Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARNICA MONTANA WHOLE; CENTELLA ASIATICA LEAF; PHOSPHORIC ACID; AMBERGRIS; SILVER NITRATE; ANAMIRTA COCCULUS FRUIT; CONIUM MACULATUM FLOWERING TOP; CANIS LUPUS FAMILIARIS MILK; THERIDION CURASSAVICUM
Active strength 3; 3; 6; 12; 12; 12; 12; 12; 12 [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
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 Vertigo Syncope Drops
Brand name suffix 2115
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA WHOLE 3 [hp_X]/59mL CENTELLA ASIATICA LEAF 3 [hp_X]/59mL PHOSPHORIC ACID 6 [hp_X]/59mL AMBERGRIS 12 [hp_X]/59mL SILVER NITRATE 12 [hp_X]/59mL ANAMIRTA COCCULUS FRUIT 12 [hp_X]/59mL CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/59mL CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/59mL THERIDION CURASSAVICUM 12 [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 C115 2026-01-09 C115 2024-01-30 C115 2024-01-30 C115
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2115-2 Vertigo Syncope Drops2115 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 63083-2115 VERTIGO SYNCOPE DROPS 2115 (VERTIGO SYNCOPE DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_6c89d8af-acd9-4b07-b8c7-14490262fe0a.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 63083-2115-2 63083211502 59 mL in 1 BOTTLE, DROPPER (63083-2115-2) 59 ml 1985-08-15 0000-00-00 No No Current