Home NDC 63083-2009-2 Anti-Stress Drops
Product NDC 63083-2009
Requested package NDC 63083-2009-2
11-digit product format 630832009
Labeler code 63083
Product ID 63083-2009_9f77406d-70e1-4a4a-bc0e-7a4b43923aa1
Type HUMAN OTC DRUG
Nonproprietary name Anti-Stress Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance APIS MELLIFERA; ARTEMISIA ANNUA FLOWERING TOP; CITRUS AURANTIUM FRUIT RIND; EPINEPHRINE; GELSEMIUM SEMPERVIRENS ROOT; NEUROTENSIN; ORNITHOGALUM UMBELLATUM FLOWERING TOP; ROYAL JELLY; STRYCHNOS IGNATII SEED
Active strength 2; 3; 6; 6; 3; 16; 6; 3; 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
Pharmacologic classes Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Bee Venoms [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
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…
Additional Listing Data#
Finished product Yes
Brand name base Anti-Stress Drops
Brand name suffix 2009
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA 2 [hp_X]/59mL ARTEMISIA ANNUA FLOWERING TOP 3 [hp_X]/59mL ROYAL JELLY 6 [hp_X]/59mL GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/59mL CITRUS AURANTIUM FRUIT RIND 3 [hp_X]/59mL ORNITHOGALUM UMBELLATUM FLOWERING TOP 16 [hp_X]/59mL EPINEPHRINE 6 [hp_X]/59mL STRYCHNOS IGNATII SEED 3 [hp_X]/59mL NEUROTENSIN 6 [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 C9 2026-01-09 C9 2024-01-30 C9 2024-01-30 C9
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2009-2 Anti-Stress Drops2009 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 63083-2009 ANTI-STRESS DROPS 2009 (ANTI-STRESS DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_3557c501-66d9-49eb-8996-028ed8274e29.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 63083-2009-2 63083200902 59 mL in 1 BOTTLE, DROPPER (63083-2009-2) 59 ml 1985-08-15 0000-00-00 No No Current