Home NDC 63083-2063-2 Substance Abuse Drops
Product NDC 63083-2063
Requested package NDC 63083-2063-2
11-digit product format 630832063
Labeler code 63083
Product ID 63083-2063_a8f36118-025c-47db-801b-609ece4c07a2
Type HUMAN OTC DRUG
Nonproprietary name Substance Abuse Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance AVENA SATIVA FLOWERING TOP; VALERIAN; APOCYNUM CANNABINUM ROOT; NUTMEG; COFFEA ARABICA SEED, ROASTED; STRYCHNOS NUX-VOMICA SEED; TOBACCO LEAF; WORMWOOD; ANTIMONY POTASSIUM TARTRATE; GOLD; HYOSCYAMUS NIGER; GONORRHEAL URETHRAL SECRETION HUMAN; SUCROSE; BETA-ENDORPHIN HUMAN
Active strength 2; 2; 3; 3; 3; 3; 4; 6; 6; 6; 60; 60; 60; 8 [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; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [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…
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 Substance Abuse Drops
Brand name suffix 2063
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVENA SATIVA FLOWERING TOP 2 [hp_X]/59mL VALERIAN 2 [hp_X]/59mL APOCYNUM CANNABINUM ROOT 3 [hp_X]/59mL NUTMEG 3 [hp_X]/59mL COFFEA ARABICA SEED, ROASTED 3 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED 3 [hp_X]/59mL TOBACCO LEAF 4 [hp_X]/59mL WORMWOOD 6 [hp_X]/59mL ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/59mL GOLD 6 [hp_X]/59mL HYOSCYAMUS NIGER 60 [hp_X]/59mL GONORRHEAL URETHRAL SECRETION HUMAN 60 [hp_X]/59mL SUCROSE 60 [hp_X]/59mL BETA-ENDORPHIN HUMAN 8 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 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 C63 2026-01-09 C63 2024-01-30 C63 2024-01-30 C63
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2063-2 Substance Abuse Drops2063 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 63083-2063 SUBSTANCE ABUSE DROPS 2063 (SUBSTANCE ABUSE DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_61f8263d-6f72-442f-a09e-57daf7226cc7.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 63083-2063-2 63083206302 59 mL in 1 BOTTLE, DROPPER (63083-2063-2) 59 ml 1985-08-15 0000-00-00 No No Current