Home NDC 63083-5016-2 Myocardial Drops
Product NDC 63083-5016
Requested package NDC 63083-5016-2
11-digit product format 630835016
Labeler code 63083
Product ID 63083-5016_a6017d58-a87b-4c61-8e09-98e56de5422f
Type HUMAN OTC DRUG
Nonproprietary name Myocardial Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance SELENICEREUS GRANDIFLORUS STEM; TERMINALIA ARJUNA WHOLE; VALERIAN; CONVALLARIA MAJALIS; VERATRUM ALBUM ROOT; SODIUM TETRACHLOROAURATE; SPIGELIA MARILANDICA ROOT; GARLIC; HAWTHORN LEAF WITH FLOWER; DIGITALIS; BEEF HEART
Active strength 3; 3; 3; 4; 4; 5; 5; 6; 6; 6; 6 [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; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant 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 Myocardial Drops
Brand name suffix 5016
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SELENICEREUS GRANDIFLORUS STEM 3 [hp_X]/59mL TERMINALIA ARJUNA WHOLE 3 [hp_X]/59mL VALERIAN 3 [hp_X]/59mL CONVALLARIA MAJALIS 4 [hp_X]/59mL VERATRUM ALBUM ROOT 4 [hp_X]/59mL SODIUM TETRACHLOROAURATE 5 [hp_X]/59mL SPIGELIA MARILANDICA ROOT 5 [hp_X]/59mL GARLIC 6 [hp_X]/59mL HAWTHORN LEAF WITH FLOWER 6 [hp_X]/59mL DIGITALIS 6 [hp_X]/59mL BEEF HEART 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-09 HMD 2026-01-09 HMD 2024-01-30 HMD 2024-01-30 HMD
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-5016-2 Myocardial Drops5016 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 63083-5016 MYOCARDIAL DROPS 5016 (MYOCARDIAL DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_23ca328e-cd71-49bb-b289-fcf50e3846b4.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 63083-5016-2 63083501602 59 mL in 1 BOTTLE, DROPPER (63083-5016-2) 59 ml 1985-08-15 0000-00-00 No No Current