Home NDC 63083-2051-2 Abdominal Pain Drops
Product NDC 63083-2051
Requested package NDC 63083-2051-2
11-digit product format 630832051
Labeler code 63083
Product ID 63083-2051_d726dade-f77f-4db7-a445-08ae30d01b06
Type HUMAN OTC DRUG
Nonproprietary name Abdominal Pain Drops
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARTEMISIA ANNUA FLOWERING TOP; LYCOPODIUM CLAVATUM SPORE; ACTIVATED CHARCOAL; SODIUM SULFATE; BOS TAURUS SOLAR PLEXUS; TRIPE; SUS SCROFA PARASYMPATHETIC NERVE; HYDROCHLORIC ACID; STRYCHNOS NUX-VOMICA SEED
Active strength 3; 5; 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
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage 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 Abdominal Pain Drops
Brand name suffix 2051
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARTEMISIA ANNUA FLOWERING TOP 3 [hp_X]/59mL LYCOPODIUM CLAVATUM SPORE 5 [hp_X]/59mL ACTIVATED CHARCOAL 6 [hp_X]/59mL SODIUM SULFATE 6 [hp_X]/59mL BOS TAURUS SOLAR PLEXUS 6 [hp_X]/59mL TRIPE 6 [hp_X]/59mL SUS SCROFA PARASYMPATHETIC NERVE 6 [hp_X]/59mL HYDROCHLORIC ACID 12 [hp_X]/59mL STRYCHNOS NUX-VOMICA SEED 30 [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 C51 2026-01-09 C51 2024-01-30 C51 2024-01-30 C51
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2051-2 Abdominal Pain Drops2051 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 63083-2051 ABDOMINAL PAIN DROPS 2051 (ABDOMINAL PAIN DROPS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220215_f1b1dde6-bb37-4774-a58c-b4f648f9c2b5.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 63083-2051-2 63083205102 59 mL in 1 BOTTLE, DROPPER (63083-2051-2) 59 ml 1985-08-15 0000-00-00 No No Current