Indications and uses
To relieve the symptoms of lightheadedness.
To relieve the symptoms of lightheadedness.
Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.
DUBOISIA
To relieve the symptoms of lightheadedness.
Keep this and all medicines out of reach of children.
Indications:
DUBOISIA Lightheadedness
If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.
Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.
Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.
Sucrose/Lactose
The OTC potency range of DUBOISIA is 4x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.
All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.
‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.
Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0740640303801 | GTIN-13: 0740640303801 EAN-13: 0740640303801 GTIN-12: 740640303801 UPC-A: 740640303801 GTIN storage (14 digits): 00740640303801 | Duboisia.jpg |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71919-260 | 71919-260-07, 71919-260-08, 71919-260-09, 71919-260-10 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| DUBOISIA MYOPOROIDES LEAF | 9T6E6S5L3D | ACTIB |
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 |
|---|---|---|---|---|---|---|
| dad03971-21bf-1c56-e053-2a95a90a4dc7 | 453abd2f-4a89-4b21-8f63-e505e42af544 | 2022-03-22 | Warnings | 453abd2f-4a89-4b21-8f63-e505e42af544 |
Adverse event summaries are temporarily unavailable. Other product information remains available.