Home NDC 43406-0685 Imucode
Product NDC 43406-0685
11-digit product format 434060685
Labeler code 43406
Product ID 43406-0685_3d04e729-a756-4fd0-a848-a76b7d70f5f9
Type HUMAN OTC DRUG
Nonproprietary name Astragalus, Hydrastis, Adrenalinum, Thyroidinum, Pituitarum Posterium, Arsenicum Alb, Baptisia, Baryta Carb, Baryta Mur, Bromium, Candida Alb, Ceanothus, Chininum Sulph, Conium, Hepar Sulph Calc, Ignatia, Indium, Iodium, Merc Solub, Phytolacca, Sulphur
Dosage form LIQUID
Route ORAL
Labeler Natural Creations, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-06-13
Substance ARSENIC TRIOXIDE; ASTRAGALUS NUTTALLII LEAF; BAPTISIA TINCTORIA WHOLE; BARIUM CARBONATE; BARIUM CHLORIDE DIHYDRATE; BROMINE; CALCIUM SULFIDE; CANDIDA ALBICANS; CEANOTHUS AMERICANUS LEAF; CONIUM MACULATUM FLOWERING TOP; EPINEPHRINE; GOLDENSEAL; INDIUM; IODINE; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; QUININE SULFATE; STRYCHNOS IGNATII SEED; SULFUR; SUS SCROFA PITUITARY GLAND, POSTERIOR; THYROID
Active strength 30; 12; 12; 12; 12; 12; 12; 30; 12; 12; 9; 8; 12; 12; 30; 12; 12; 12; 12; 9; 9 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 · 16 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 43406-0685-1 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 43406-0685-1 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 43406-0685-1 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 43406-0685-1 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 43406-0685-1 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 43406-0685-1 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 43406-0685-1 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 43406-0685-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Imucode
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GOLDENSEAL 30 [hp_C]/mL EPINEPHRINE 12 [hp_X]/mL THYROID 12 [hp_X]/mL SUS SCROFA PITUITARY GLAND, POSTERIOR 12 [hp_X]/mL ASTRAGALUS NUTTALLII LEAF 12 [hp_X]/mL BAPTISIA TINCTORIA WHOLE 12 [hp_X]/mL BARIUM CARBONATE 12 [hp_X]/mL BARIUM CHLORIDE DIHYDRATE 30 [hp_C]/mL BROMINE 12 [hp_X]/mL CEANOTHUS AMERICANUS LEAF 12 [hp_X]/mL QUININE SULFATE 9 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/mL CALCIUM SULFIDE 12 [hp_X]/mL STRYCHNOS IGNATII SEED 12 [hp_X]/mL INDIUM 30 [hp_C]/mL IODINE 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL SULFUR 12 [hp_X]/mL ARSENIC TRIOXIDE 12 [hp_X]/mL CANDIDA ALBICANS 9 [hp_X]/mL MERCURIUS SOLUBILIS 9 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 21 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43406-0685-1 Imucode 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43406-0685 IMUCODE (ASTRAGALUS, HYDRASTIS, ADRENALINUM, THYROIDINUM, PITUITARUM POSTERIUM, ARSENICUM ALB, BAPTISIA, BARYTA CARB, BARYTA MUR, BROMIUM, CANDIDA ALB, CEANOTHUS, CHININUM SULPH, CONIUM, HEPAR SULPH CALC, IGNATIA, INDIUM, IODIUM, MERC SOLUB, PHYTOLACCA, SULPHUR) LIQUID [NATURAL CREATIONS, INC] 1 Current NDC, Legacy NDC, 1 package rows 20230111_be30901c-0673-4af0-8128-83ed59ff04b1.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Imucode ASTRAGALUS, HYDRASTIS, ADRENALINUM, THYROIDINUM, PITUITARUM POSTERIUM, ARSENICUM ALB, BAPTISIA, BARYTA CARB, BARYTA MUR, BROMIUM, CANDIDA ALB, CEANOTHUS, CHININUM SULPH, CONIUM, HEPAR SULPH CALC, IGNATIA, INDIUM, IODIUM, MERC SOLUB, PHYTOLACCA, SULPHUR Natural Creations, Inc be30901c-0673-4af0-8128-83ed59ff04b1 2018-12-21 Warnings Exact identifier ndc (product): 43406-0685
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43406-0685-1 43406068501 30 mL in 1 BOTTLE, DROPPER (43406-0685-1) 30 ml 2018-06-13 0000-00-00 No No Current