Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
(in each drop): 100% of Nux Vomica 200C.
May temporarily relieve digestive issues, especially from overeating.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
In case of overdose, get medical help or contact a Poison Control Center right away.
Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
May temporarily relieve digestive issues, especially from overeating.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Demineralized water, 20% Ethanol.
Dist. by Energique, Inc.
201 Apple Blvd
Woodbine, IA 51579 800-869-8078
ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
NUX VOM
200C
1 fl. oz. (30 ml)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0170-1 | 2024-04-08 | C162847 | 48780-1 | ba0f9c33-134a-a910-e053-dadaa90a0b85 | DRUG FACTS: |
| 44911-0170-1 | 2024-01-30 | C162847 | 48780-1 | ba0f9c33-134a-a910-e053-dadaa90a0b85 | DRUG FACTS: |
| 44911-0170-1 | 2022-03-14 | C162847 | 48780-1 | ba0f9c33-134a-a910-e053-dadaa90a0b85 | DRUG FACTS: |
| 44911-0170-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-134a-a910-e053-dadaa90a0b85 | DRUG FACTS: |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0170-1 | Nux Vom | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 5 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0170 | NUX VOM (NUX VOMICA) LIQUID [ENERGIQUE, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240410_e3298f57-0a6b-4e35-876d-2ffd21673b64.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| STRYCHNOS NUX-VOMICA SEED | ACTIVE INGREDIENT | 269XH13919 | 1 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE MOIETY | 269XH13919 | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 44911-0170 | 44911-0170-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nux Vom | NUX VOMICA | Energique, Inc. | e3298f57-0a6b-4e35-876d-2ffd21673b64 | 2024-04-08 | Warnings | 44911-0170-1 44911-0170 44911017001 1cd725bf-aa37-4532-9ebd-4a2fc33a0598 e3298f57-0a6b-4e35-876d-2ffd21673b64 |
Adverse event summaries are temporarily unavailable. Other product information remains available.