Home NDC 63083-9240-1 Rheum Combination
Product NDC 63083-9240
Requested package NDC 63083-9240-1
11-digit product format 630839240
Labeler code 63083
Product ID 63083-9240_b89d688f-e7f1-49a1-b55e-c193d2adfd7b
Type HUMAN OTC DRUG
Nonproprietary name Rheum Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ALOE; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; FRANGULA ALNUS BARK; GRAPHITE; MEDICAGO SATIVA WHOLE; RHEUM OFFICINALE STEM; SENNA LEAF; STAR ANISE; STRYCHNOS NUX-VOMICA SEED; VERONICASTRUM VIRGINICUM WHOLE
Active strength 4; 4; 6; 2; 8; 1; 1; 1; 1; 4; 1 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL
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 Rheum Combination
Brand name suffix 9240
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STAR ANISE 1 [hp_X]/29.5mL VERONICASTRUM VIRGINICUM WHOLE 1 [hp_X]/29.5mL MEDICAGO SATIVA WHOLE 1 [hp_X]/29.5mL RHEUM OFFICINALE STEM 1 [hp_X]/29.5mL SENNA LEAF 1 [hp_X]/29.5mL FRANGULA ALNUS BARK 2 [hp_X]/29.5mL ALOE 4 [hp_X]/29.5mL BRYONIA ALBA ROOT 4 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 4 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/29.5mL GRAPHITE 8 [hp_X]/29.5mL
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 R240 2026-01-09 R240 2024-01-30 R240 2024-01-30 R240
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9240-1 Rheum Combination9240 29.5 mL in 1 BOTTLE, DROPPER LIQUID 29.5 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-9240 RHEUM COMBINATION 9240 (RHEUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_f65a41b7-5931-4c62-89a3-7b255757527f.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 63083-9240-1 63083924001 29.5 mL in 1 BOTTLE, DROPPER (63083-9240-1) 29.5 ml 1985-08-15 0000-00-00 No No Current