Eazol
- Product NDC
- 50845-0131
- 11-digit product format
- 508450131
- Labeler code
- 50845
- Product ID
- 50845-0131_fd0677ba-1a4e-4d2c-aef0-73d6ebeade55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Arsenicum album, Coffea cruda, Euphorbium officinarum, Gnaphalium polycephalum, Hypericum perforatum, Magnesia phosphorica, Passiflora incarnata, Ranunculus bulbosus,
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-04-15
- Marketing end
- 2026-06-30
- Substance
- ACONITUM NAPELLUS; ARABICA COFFEE BEAN; ARSENIC TRIOXIDE; EUPHORBIA RESINIFERA RESIN; HYPERICUM PERFORATUM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA TOP; PSEUDOGNAPHALIUM OBTUSIFOLIUM; RANUNCULUS BULBOSUS
- Active strength
- 200; 200; 200; 4; 200; 12; 1; 3; 3 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Eazol
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACONITUM NAPELLUS | 200 [hp_C]/mL |
| ARABICA COFFEE BEAN | 200 [hp_C]/mL |
| ARSENIC TRIOXIDE | 200 [hp_C]/mL |
| EUPHORBIA RESINIFERA RESIN | 4 [hp_X]/mL |
| HYPERICUM PERFORATUM | 200 [hp_C]/mL |
| MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE | 12 [hp_X]/mL |
| PASSIFLORA INCARNATA TOP | 1 [hp_X]/mL |
| PSEUDOGNAPHALIUM OBTUSIFOLIUM | 3 [hp_X]/mL |
| RANUNCULUS BULBOSUS | 3 [hp_X]/mL |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | U0NQ8555JD, 3SW678MX72, S7V92P67HO, 1TI1O9028K, XK4IUX8MNB, HF539G9L3Q, CLF5YFS11O, 36XQ854NWW, AEQ8NXJ0MB |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0131-1 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-c9fb-8e05-e053-dbdaa90a074a | DRUG FACTS: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0131-1 | Eazol | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0131 | EAZOL (ACONITUM NAPELLUS, ARSENICUM ALBUM, COFFEA CRUDA, EUPHORBIUM OFFICINARUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PASSIFLORA INCARNATA, RANUNCULUS BULBOSUS,) SPRAY [LIDDELL LABORATORIES, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20110425_f0942edb-cb93-41f9-8ae5-df669df94db4.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50845-0131-1 | 50845013101 | 30 mL in 1 BOTTLE, SPRAY (50845-0131-1) | 30 ml | 2011-04-15 | 2026-06-30 | No | No | Historical |