Home NDC 43857-0331-01 NDC 43857-0331-01 - ADRENOPLEX This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 43857-0331
Requested NDC 43857-0331-01
Package NDCs from labels 43857-0331-1, 43857-0331-01
Manufacturer BioActive Nutritional, Inc. | Apotheca Company
Effective date 2025-12-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43857-0331-1 ADRENOPLEX 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43857-0331 ADRENOPLEX (CHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), GLANDULA SUPRARENALIS BOVINE, SPLEEN (SUIS), CARDUUS MARIANUS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20161206_3c53c23e-7654-4e46-acf1-edb0d605ff3b.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BOS TAURUS ADRENAL GLAND ACTIVE INGREDIENT M2776SWB29 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 CHELIDONIUM MAJUS ACTIVE INGREDIENT 7E889U5RNN ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 ECHINACEA ANGUSTIFOLIA ACTIVE INGREDIENT VB06AV5US8 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 LYCOPODIUM CLAVATUM SPORE ACTIVE INGREDIENT C88X29Y479 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 MILK THISTLE ACTIVE INGREDIENT U946SH95EE ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 PHOSPHORIC ACID ACTIVE INGREDIENT E4GA8884NN ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 SODIUM CHLORIDE ACTIVE INGREDIENT 451W47IQ8X ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 SUS SCROFA SPLEEN ACTIVE INGREDIENT 92AMN5J79Y ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 BOS TAURUS ADRENAL GLAND ACTIVE MOIETY M2776SWB29 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 CHELIDONIUM MAJUS ACTIVE MOIETY 7E889U5RNN ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 CHLORIDE ION ACTIVE MOIETY Q32ZN48698 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 ECHINACEA ANGUSTIFOLIA ACTIVE MOIETY VB06AV5US8 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 LYCOPODIUM CLAVATUM SPORE ACTIVE MOIETY C88X29Y479 ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 MILK THISTLE ACTIVE MOIETY U946SH95EE ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 PHOSPHORIC ACID ACTIVE MOIETY E4GA8884NN ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 SUS SCROFA SPLEEN ACTIVE MOIETY 92AMN5J79Y ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ADRENOPLEX (NOT APPLICABLE) LIQUID [BIOACTIVE NUTRITIONAL, INC.] 1
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 174 of 245 · 4,895 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Instant Hand Sanitizing Wipe ETHYL ALCOHOL McKesson 9f51a505-2d55-5c49-e053-2a95a90a2403 2024-10-14 Warnings Exact identifier unii: 3K9958V90M Eye Wash WATER SOLUTION Kroger Company 354402ad-581d-47e7-9fd3-933bef281ff4 2024-10-11 Warnings Exact identifier unii: 059QF0KO0R Insect Sting Relief Pad BENZOCAINE, ALCOHOL Hubei Changjian Medical Products Co., Ltd. 6a269982-0e25-4c09-aef1-0b398bdc5ed4 2024-10-11 Warnings Exact identifier unii: 3K9958V90M Antiseptic Hand Sanitizer ALCOHOL Hubei Changjian Medical Products Co., Ltd. b7f00c15-852f-45ce-9c60-70e0b80234f5 2024-10-11 Warnings Exact identifier unii: 3K9958V90M Eye Wash WATER Hubei Changjian Medical Products Co., Ltd. d57e1c5b-1edc-4a94-88bc-f9ecf347b7ea 2024-10-11 Warnings Exact identifier unii: 059QF0KO0R Antiseptic ETHANOL McKesson 6637290d-6ae4-5a83-e053-2991aa0a81c6 2024-10-11 Warnings Exact identifier unii: 3K9958V90M Alcohol Disinfecting Wipe ALCOHOL McKesson Medical-Surgical 64a0063d-a5da-4a46-9dca-16e4dbdac85c 2024-10-11 Warnings Exact identifier unii: 3K9958V90M Sodium Chloride SODIUM CHLORIDE Fresenius Kabi USA, LLC c44b0fdb-33df-4747-b443-5fb4deb456cb 2024-10-11 Warnings, Adverse reactions Exact identifier unii: 451W47IQ8X Bacteriostatic Sodium Chloride SODIUM CHLORIDE Fresenius Kabi USA, LLC e5e325d1-0d58-40c9-9645-3ae402ff9d92 2024-10-11 Warnings, Adverse reactions Exact identifier unii: 451W47IQ8X Mist ALCOHOL Derma Glove 2a0bcc4e-5114-4afc-91cb-cb4816a63db2 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand LOTION Derma Glove ba9611a3-e2a4-4835-9ffe-aafe85a7cb9c 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove 45d130c9-0835-45bb-b525-86a2119c87d1 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Mist ALCOHOL Derma Glove b5bfd7f0-0f96-459e-84d4-24b2081ae46f 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove e2f89d56-5624-4a94-8151-1edb508232ac 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Recovery ALCOHOL Derma Glove 06f74478-57aa-4b8d-b888-55e1ee4fbd45 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove d3926f48-3a42-42df-a850-47b3914ba3b6 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Mist ALCOHOL Derma Glove 7c21ee1c-ce2a-464b-8269-cdb3e59db094 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand LOTION Derma Glove bcd71f37-63aa-4ad9-a9be-e5519c7e66e7 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Hand Relief LOTION Derma Glove ffdfb167-0efa-4cd8-afdf-e1ff69ee6252 2024-10-09 Warnings Exact identifier unii: 3K9958V90M Mist ALCOHOL Derma Glove 11c2939c-e77a-48f6-949c-9d508714012b 2024-10-09 Warnings Exact identifier unii: 3K9958V90M
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.