KALI SULPHURICUM
- Manufacturer
- STANDARD HOMEOPATHIC COMPANY
- Effective date
- 2019-12-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:52:01
Label at a glance#
ProductKALI SULPHURICUM
Active ingredientPOTASSIUM SULFATE
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
RUNNY NOSE OR SKIN ERUPTIONS
WARNINGS SECTION
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. To be used according to label indications and/or standard homeopathic indications
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all medicines out of the reach of children.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: ADULTS: Dissolve 4 tablets under the tongue 4 times a day.
CHILDREN: 2 tablets as above.
INACTIVE INGREDIENT SECTION
In a base of Acacia Gum and Lactose N.F.
OTC - QUESTIONS SECTION
800-624-9659
OTC - ACTIVE INGREDIENT SECTION
KALI SULPH. 6X
OTC - PURPOSE SECTION
RUNNY NOSE OR SKIN ERUPTIONS
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Principal Display Panel -- 500 Tablet Bottle
Made according to the Homeopathic Pharmacopoeia of the United States since 1903.
Warnings: 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
Standard Homeopathic
Made in the USA Since 1903
NDC # 0360-0243-02
Homeopathic Medicine
KALI SULPH. 6X
RUNNY NOSE OR SKIN ERUPTIONS
500 TABLETS
DIRECTIONS: ADULTS: Dissolve 4 tablets under the tongue 4 times a day.
CHILDREN: 2 tablets as above.
In a base of Acacia Gum and Lactose N.F.
3 00360 02432 7
Lot #: XXXXXX
Products#
Every source-derived product name is available through these pages.
- KALI SULPHURICUM
- KALI SULPH
- POTASSIUM SULFATE
- SULFATE ION
- ACACIA
- LACTOSE MONOHYDRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0360-0243 | 0360-0243-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| POTASSIUM SULFATE | 1K573LC5TV | ACTIB |
| ACACIA | 5C5403N26O | IACT |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 999f1ee4-545e-e6a8-e053-2a95a90aca40 | 504c1ada-607a-4d49-e054-00144ff8d46c | 2019-12-13 | Warnings | 999f1ee4-545e-e6a8-e053-2a95a90aca40 504c1ada-607a-4d49-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.