Home NDC 63083-9203-1 Aletris Combination
Product NDC 63083-9203
Requested package NDC 63083-9203-1
11-digit product format 630839203
Labeler code 63083
Product ID 63083-9203_eb4d236e-99a3-435e-b20b-b13d8b1f5086
Type HUMAN OTC DRUG
Nonproprietary name Aletris Combination
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ALETRIS FARINOSA ROOT; ANAMIRTA COCCULUS FRUIT; IRON; FERRIC CATION; FERROSOFERRIC PHOSPHATE; FERROUS CATION; CHAMAELIRIUM LUTEUM ROOT; SODIUM CHLORIDE; PICRIC ACID; SEPIA OFFICINALIS JUICE; QUININE ARSENITE; POTASSIUM CARBONATE
Active strength 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8 [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 Antimalarial [EPC], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
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 Aletris Combination
Brand name suffix 9203
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALETRIS FARINOSA ROOT 4 [hp_X]/29.5mL ANAMIRTA COCCULUS FRUIT 4 [hp_X]/29.5mL IRON 6 [hp_X]/29.5mL FERRIC CATION 6 [hp_X]/29.5mL FERROSOFERRIC PHOSPHATE 6 [hp_X]/29.5mL FERROUS CATION 6 [hp_X]/29.5mL CHAMAELIRIUM LUTEUM ROOT 6 [hp_X]/29.5mL SODIUM CHLORIDE 6 [hp_X]/29.5mL PICRIC ACID 6 [hp_X]/29.5mL SEPIA OFFICINALIS JUICE 6 [hp_X]/29.5mL QUININE ARSENITE 8 [hp_X]/29.5mL POTASSIUM CARBONATE 8 [hp_X]/29.5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 R203 2026-01-09 R203 2024-01-30 R203 2024-01-30 R203
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-9203-1 Aletris Combination9203 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 63083-9203 ALETRIS COMBINATION 9203 (ALETRIS COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220210_87ae7310-927b-48fe-b659-6f93dad62363.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 63083-9203-1 63083920301 29.5 mL in 1 BOTTLE, DROPPER (63083-9203-1) 29.5 ml 1985-08-15 0000-00-00 No No Current