Allergen
- Product NDC
- 43857-0241
- Requested package NDC
- 43857-0241-1
- 11-digit product format
- 438570241
- Labeler code
- 43857
- Product ID
- 43857-0241_4a34bfaf-27e7-4a03-b124-dac29340b020
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium Gluconate, Glandula Suprarenalis Bovine, Hepar Bovine, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphorus, Peanut, Black Walnut, Juglans Regia, Almond, Cashew, Coconut, Pecan, Brazil Nut, Lycopersicum Esculentum, Potato, Black Pepper, Eggplant, Gossypium Herbaceum, Flax, Parmesan Cheese, Milk, Beef, Lamb, Pork, Chicken, Egg, Beans, Allium Cepa, Malus Pumila, Flos, Triticum Aestivum, Banana, Fragaria Vesca, Citrus Sinensis, Cod, Tuna, Salmon, Limulus, Oyster, Shrimp, Cortisone Aceticum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-09-26
- Marketing end
- 2023-11-16
- Substance
- POTASSIUM GLUCONATE; BOS TAURUS ADRENAL GLAND; BEEF LIVER; ARSENIC TRIOXIDE; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; PEANUT; BLACK WALNUT; ENGLISH WALNUT; ALMOND; CASHEW; COCONUT; PECAN; BRAZIL NUT; SOLANUM LYCOPERSICUM; POTATO; BLACK PEPPER; EGGPLANT; LEVANT COTTON SEED; FLAX SEED; SESAME SEED; CASEIN, LACTOCOCCUS LACTIS CULTURED; COW MILK; BEEF; LAMB; PORK; CHICKEN; EGG; KIDNEY BEAN; ONION; MALUS PUMILA FLOWER; WHEAT; BANANA; ALPINE STRAWBERRY; ORANGE; COD, UNSPECIFIED; TUNA, UNSPECIFIED; SALMON, UNSPECIFIED; LIMULUS POLYPHEMUS; OYSTER, UNSPECIFIED; SHRIMP, UNSPECIFIED; CORTISONE ACETATE; HISTAMINE DIHYDROCHLORIDE; HYALURONIDASE; INTERFERON .GAMMA. PORCINE RECOMBINANT; SEROTONIN HYDROCHLORIDE
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 43857-0241 | 43857-0241-1 | D | Discontinued by firm | 2026-10-05 |
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.
| 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… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43857-0241-1 | 43857024101 | 30 mL in 1 BOTTLE, DROPPER (43857-0241-1) | 30 ml | 2017-03-30 | 2023-11-16 | No | No | Current |