Home NDC 63083-9240 Rheum Combination
Product NDC 63083-9240
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 openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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 4 [hp_X]/29.5mL VERONICASTRUM VIRGINICUM WHOLE 4 [hp_X]/29.5mL MEDICAGO SATIVA WHOLE 6 [hp_X]/29.5mL RHEUM OFFICINALE STEM 2 [hp_X]/29.5mL SENNA LEAF 8 [hp_X]/29.5mL FRANGULA ALNUS BARK 1 [hp_X]/29.5mL ALOE 1 [hp_X]/29.5mL BRYONIA ALBA ROOT 1 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 1 [hp_X]/29.5mL CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X]/29.5mL GRAPHITE 1 [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# 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
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