Home NDC 63083-2083-2 Angina Drops
Product NDC 63083-2083
Requested package NDC 63083-2083-2
11-digit product format 630832083
Labeler code 63083
Product ID 63083-2083_b4cee559-3d7f-4b9b-b0f1-f1f218046d57
Type HUMAN OTC DRUG
Nonproprietary name Angina Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance HAWTHORN LEAF WITH FLOWER; SELENICEREUS GRANDIFLORUS STEM; KALMIA LATIFOLIA LEAF; PHOSPHORUS; ARSENIC TRIOXIDE; DIGITALIS; NITROGLYCERIN; DRIMIA MARITIMA BULB; GELSEMIUM SEMPERVIRENS ROOT; SPIGELIA MARILANDICA ROOT; POTASSIUM CARBONATE; ARNICA MONTANA WHOLE
Active strength 2; 3; 3; 5; 6; 6; 6; 6; 6; 6; 12; 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; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE]
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 Angina Drops
Brand name suffix 2083
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HAWTHORN LEAF WITH FLOWER 2 [hp_X]/59mL SELENICEREUS GRANDIFLORUS STEM 3 [hp_X]/59mL KALMIA LATIFOLIA LEAF 3 [hp_X]/59mL PHOSPHORUS 5 [hp_X]/59mL ARSENIC TRIOXIDE 6 [hp_X]/59mL DIGITALIS 6 [hp_X]/59mL NITROGLYCERIN 6 [hp_X]/59mL DRIMIA MARITIMA BULB 6 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/59mL SPIGELIA MARILANDICA ROOT 6 [hp_X]/59mL POTASSIUM CARBONATE 12 [hp_X]/59mL ARNICA MONTANA WHOLE 30 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 C83 2026-01-09 C83 2024-01-30 C83 2024-01-30 C83
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2083-2 Angina Drops2083 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 63083-2083 ANGINA DROPS 2083 (ANGINA DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_99516597-9f59-4123-bd35-a4a73dd54d2d.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 63083-2083-2 63083208302 59 mL in 1 BOTTLE, DROPPER (63083-2083-2) 59 ml 1985-08-15 0000-00-00 No No Current