Home NDC 63083-7005-1 RET Kidney
Product NDC 63083-7005
Requested package NDC 63083-7005-1
11-digit product format 630837005
Labeler code 63083
Product ID 63083-7005_ce57b1da-4d72-4c34-b5d4-ed9c7d3d4c7c
Type HUMAN OTC DRUG
Nonproprietary name RET Kidney
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance POPULUS TREMULA FLOWERING TOP; MIMULUS GUTTATUS FLOWERING TOP; PINUS SYLVESTRIS FLOWERING TOP; CALCIUM SULFATE ANHYDROUS; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; SILVER NITRATE; GOLD; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GRAPHITE; STRYCHNOS IGNATII SEED; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; SEPIA OFFICINALIS JUICE
Active strength 3; 3; 3; 3; 3; 30; 30; 30; 30; 30; 30; 30; 30 [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; [hp_X]/29.5mL; [hp_X]/29.5mL
Pharmacologic classes Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], 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 RET Kidney
Brand name suffix 7005
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POPULUS TREMULA FLOWERING TOP 3 [hp_X]/29.5mL MIMULUS GUTTATUS FLOWERING TOP 3 [hp_X]/29.5mL PINUS SYLVESTRIS FLOWERING TOP 3 [hp_X]/29.5mL CALCIUM SULFATE ANHYDROUS 3 [hp_X]/29.5mL POTASSIUM PHOSPHATE, UNSPECIFIED FORM 3 [hp_X]/29.5mL SILVER NITRATE 30 [hp_X]/29.5mL GOLD 30 [hp_X]/29.5mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_X]/29.5mL GRAPHITE 30 [hp_X]/29.5mL STRYCHNOS IGNATII SEED 30 [hp_X]/29.5mL LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/29.5mL PHOSPHORUS 30 [hp_X]/29.5mL SEPIA OFFICINALIS JUICE 30 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 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 RET5 2026-01-09 RET5 2024-01-30 RET5 2024-01-30 RET5
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-7005-1 RET Kidney7005 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 63083-7005 RET KIDNEY 7005 (RET KIDNEY) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220209_017f4c37-3eec-4078-9ce6-aca52fd4974d.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 63083-7005-1 63083700501 29.5 mL in 1 BOTTLE, DROPPER (63083-7005-1) 29.5 ml 1985-08-15 0000-00-00 No No Current