Home NDC 63083-9307-1 Uric Acid Combination
Product NDC 63083-9307
Requested package NDC 63083-9307-1
11-digit product format 630839307
Labeler code 63083
Product ID 63083-9307_f1791c2d-4b6a-4f62-9eec-defc383f3475
Type HUMAN OTC DRUG
Nonproprietary name Uric Acid Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance SODIUM CARBONATE; COLCHICUM AUTUMNALE BULB; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS LEAF; FERROSOFERRIC PHOSPHATE; LITHIUM CARBONATE; GLUTAMINE; 1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA; URIC ACID
Active strength 3; 4; 6; 6; 8; 8; 12; 12; 12 [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], Amino Acid [EPC], Amino Acids [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Mood Stabilizer [EPC], 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 Uric Acid Combination
Brand name suffix 9307
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CARBONATE 3 [hp_X]/29.5mL COLCHICUM AUTUMNALE BULB 4 [hp_X]/29.5mL STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/29.5mL TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/29.5mL FERROSOFERRIC PHOSPHATE 8 [hp_X]/29.5mL LITHIUM CARBONATE 8 [hp_X]/29.5mL GLUTAMINE 12 [hp_X]/29.5mL 1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA 12 [hp_X]/29.5mL URIC ACID 12 [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 R307 2026-01-09 R307 2024-01-30 R307 2024-01-30 R307
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9307-1 Uric Acid Combination9307 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 63083-9307 URIC ACID COMBINATION 9307 (URIC ACID COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220211_3f136f86-a9ed-4a04-98cb-81abe33cd181.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 63083-9307-1 63083930701 29.5 mL in 1 BOTTLE, DROPPER (63083-9307-1) 29.5 ml 1985-08-15 0000-00-00 No No Current