Pancreapar
- Product NDC
- 44911-0681
- 11-digit product format
- 449110681
- Labeler code
- 44911
- Product ID
- 44911-0681_373c3034-7f21-4ca8-b09e-469e3e85f899
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Syzygium Jambolanum, Glandula Suprarenalis Suis, Hydrastis Canadensis, Hypophysis Suis, Pancreas Suis, Phaseolus, Aceticum Acidum, Lacticum Acidum, Phosphoricum Acidum, Phosphorus, Uranium Nitricum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-08-24
- Substance
- ACETIC ACID; GOLDENSEAL; KIDNEY BEAN; LACTIC ACID, DL-; PHOSPHORIC ACID; PHOSPHORUS; SUS SCROFA ADRENAL GLAND; SUS SCROFA PANCREAS; SUS SCROFA PITUITARY GLAND; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE
- Active strength
- 12; 6; 9; 12; 12; 12; 6; 6; 6; 3; 15 [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_C]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| Q40Q9N063P | ACETIC ACID | 64-19-7 | ACETIC ACID |
| ZW3Z11D0JV | GOLDENSEAL | | GOLDENSEAL |
| M98C8416QO | KIDNEY BEAN | | KIDNEY BEAN |
| 3B8D35Y7S4 | LACTIC ACID, DL- | 50-21-5 | LACTIC ACID, DL- |
| E4GA8884NN | PHOSPHORIC ACID | 7664-38-2 | PHOSPHORIC ACID |
| 27YLU75U4W | PHOSPHORUS | 7723-14-0 | PHOSPHORUS |
| 398IYQ16YV | SUS SCROFA ADRENAL GLAND | | SUS SCROFA ADRENAL GLAND |
| 9Y3J3362RY | SUS SCROFA PANCREAS | | SUS SCROFA PANCREAS |
| L0PFEMQ1DT | SUS SCROFA PITUITARY GLAND | | SUS SCROFA PITUITARY GLAND |
| 820LSF646I | SYZYGIUM CUMINI SEED | | SYZYGIUM CUMINI SEED |
| 3V057702FY | URANYL NITRATE HEXAHYDRATE | 13520-83-7 | URANYL NITRATE HEXAHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 44911-0681-1 | 44911068101 | 30 mL in 1 BOTTLE, DROPPER (44911-0681-1) | 30 ml | 2023-08-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| DRUG FACTS: | Energique, Inc. | Apotheca Company | 2023-08-24 | HUMAN OTC DRUG LABEL | 1 |