Home NDC 63083-7007-1 RET Gallbladder
Product NDC 63083-7007
Requested package NDC 63083-7007-1
11-digit product format 630837007
Labeler code 63083
Product ID 63083-7007_b82992bf-fb5e-4189-8bc5-531d8268b0b1
Type HUMAN OTC DRUG
Nonproprietary name RET Gallbladder
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ULEX EUROPAEUS FLOWER; ELEUTHEROCOCCUS SENTICOSUS ROOT OIL; SALIX ALBA FLOWERING TOP; POTASSIUM PHOSPHATE, UNSPECIFIED FORM; COPPER; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; DATURA STRAMONIUM
Active strength 3; 3; 3; 3; 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
Pharmacologic classes Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE]
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 Gallbladder
Brand name suffix 7007
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ULEX EUROPAEUS FLOWER 3 [hp_X]/29.5mL ELEUTHEROCOCCUS SENTICOSUS ROOT OIL 3 [hp_X]/29.5mL SALIX ALBA FLOWERING TOP 3 [hp_X]/29.5mL POTASSIUM PHOSPHATE, UNSPECIFIED FORM 3 [hp_X]/29.5mL COPPER 30 [hp_X]/29.5mL LACHESIS MUTA VENOM 30 [hp_X]/29.5mL LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/29.5mL SODIUM CHLORIDE 30 [hp_X]/29.5mL DATURA STRAMONIUM 30 [hp_X]/29.5mL
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 RET7 2026-01-09 RET7 2024-01-30 RET7 2024-01-30 RET7
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-7007-1 RET Gallbladder7007 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 63083-7007 RET GALLBLADDER 7007 (RET GALLBLADDER) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220209_82bc7b50-aea3-4993-b171-919940fef297.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 63083-7007-1 63083700701 29.5 mL in 1 BOTTLE, DROPPER (63083-7007-1) 29.5 ml 1985-08-15 0000-00-00 No No Current