KALI SULPHURICUM

Manufacturer: SEVENE USA
Effective date: 2025-02-11
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 02:32:07

Label at a glance#

ProductKALI SULPHURICUM 6X

Active ingredientPOTASSIUM SULFATE

Label structure11 sections

Indications and uses

Itching rash, scaly and chapped skin, and infected skin with yellow discharge**. **C, K, CK & X are homeopathic dilutions.

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue three times a day until symptoms are relieved or as directed by a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

KALI SULPHURICUM 6X**

**C, K, CK & X are homeopathic dilutions.

TRADITIONALLY USED FOR TEMPORARY RELIEF FROM:

OTC - PURPOSE SECTION

Itching rash, scaly and chapped skin, and infected skin with yellow discharge*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

(adults/children) Dissolve 5 pellets under the tongue three times a day until symptoms are relieved or as directed by a doctor.

USES:

INDICATIONS & USAGE SECTION

Itching rash, scaly and chapped skin, and infected skin with yellow discharge**.

**C, K, CK & X are homeopathic dilutions.

WARNINGS

WARNINGS SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
In case of overdose, get medical help.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Store at room temperature.
Do not use if tamper-evidence seal is broken.
Organic verified by Alpes Control 2021/A03M216K/1.

**C, K, CK & X are homeopathic dilutions

INACTIVE INGREDIENT:

INACTIVE INGREDIENT SECTION

ORGANIC SUCROSE

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

Email us at: info@ollois.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Kali Sulphuricum_6X_80ct

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76472-4094-1	2025-02-11	C162847	48780-1	2cef2736-a032-d83d-e063-dadaa90ab31f	SEVENE USA (as PLD) - KALI SULPHURICUM 6X (76472-4094)
76472-4094-1	2025-01-30	C162847	48780-1	2cef2736-a032-d83d-e063-dadaa90ab31f	SEVENE USA (as PLD) - KALI SULPHURICUM 6X (76472-4094)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76472-4094-1	KALI SULPHURICUM6X	80 in 1 CYLINDER	PELLET	80		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76472-4094	KALI SULPHURICUM 6X (KALI SULPHURICUM) PELLET [SEVENE USA]	4	Current NDC, 1 package rows	20250213_ff0efbc2-d7ab-9783-e053-6394a90a384f.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

KALI SULPHURICUM 6X
KALI SULPHURICUM
SUCROSE
POTASSIUM SULFATE
SULFATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76472-4094	76472-4094-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
POTASSIUM SULFATE	1K573LC5TV	ACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
KALI SULPHURICUM 6X	KALI SULPHURICUM	SEVENE USA	ff0efbc2-d7ab-9783-e053-6394a90a384f	2025-02-11	Warnings	Exact identifier ndc (package): 76472-4094-1 ndc (product): 76472-4094 ndc11 (package): 76472409401 spl id: 2ddc53bf-0bf5-fb07-e063-6394a90aa1cd spl set id: ff0efbc2-d7ab-9783-e053-6394a90a384f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.