Dosage and administration
Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional
Adults: Dissolve 4 tablets under tongue 4 times a day. Children: Consult a healthcare professional
Made according to the
Homeopathic Pharmacopoeia
of the United States since 1903.
Do not use if cap band is missing or broken.
If you are pregnant or nursing, consult a licensed health
care professional before using this product.
If symptoms persist for 7 days or worsen,
contact a licensed practitioner.
Keep this and all medicines out of the reach of children.
To be used according to label indications and/or
standard homeopathic indications.
Standard Homeopathic Company
Los Angeles, CA 90061
Questions? 800-624-9659
Adults: Dissolve 4 tablets under tongue 4 times a day.
Children: Consult a healthcare professional
In a base of Acacia Gum and Lactose N.F.
PHYTOLACCA 6X
SORE THROAT OR MINOR RHEUMATIC PAIN
Standard
Homeopathic
Made in the USA Since 1903
NDC # 0360-0306-01
Homeopathic Medicine
PHYTOLACCA
6X
SORE THROAT OR
MINOR RHEUMATIC PAIN*
*Claims based on traditional homeopathic practice,
not accepted medical evidence. Not FDA evaluated.
250 TABLETS
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0360-0306 | 0360-0306-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACACIA | 5C5403N26O | IACT |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| PHYTOLACCA AMERICANA ROOT | 11E6VI8VEG | 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 |
|---|---|---|---|---|---|---|
| d27f2057-aa35-8ce2-e053-2a95a90a4a1b | 4daec9c2-8db7-57d0-e054-00144ff88e88 | 2021-12-06 | Warnings | d27f2057-aa35-8ce2-e053-2a95a90a4a1b 4daec9c2-8db7-57d0-e054-00144ff88e88 |
Adverse event summaries are temporarily unavailable. Other product information remains available.