FDA.reportPublic FDA data

Jacksons Cell Salts KALI SULPH 6X

Manufacturer
Zettl Health Inc.
Effective date
2025-06-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:54

Label at a glance#

ProductJacksons Cell Salts KALI SULPH 6X 7
Active ingredientPOTASSIUM SULFATE
Label structure12 sections

Indications and uses

Temporarily relieves: • minor skin eruptions

Dosage and administration

Use as directed. Adults and children 6 years and over: Dissolve 4 pellets under tongue 1-3 times per day.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Kali sulphuricum 6X

Purpose

OTC - PURPOSE SECTION

Kali sulphuricum -- Minor skin eruptions

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves:

• minor skin eruptions

Warnings

WARNINGS SECTION

WARNINGS

OTC - STOP USE SECTION

Stop use and ask a doctor if:

  • symptoms persist for more than 72 hours or worsen
  • new symptoms occur

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

SPL UNCLASSIFIED SECTION

*The letters “HPUS” indicate that these ingredients are officially monographed in the Homeopathic Pharmacopeia of the United States

*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

DO NOT USE IF TAMPER-EVIDENT SEAL IS BROKEN OR MISSING.

JACKSONSNATURALS.COM

Inactive Ingredients

INACTIVE INGREDIENT SECTION

sucrose

Directions

DOSAGE & ADMINISTRATION SECTION

  • Use as directed.
  • Adults and children 6 years and over: Dissolve 4 pellets under tongue 1-3 times per day.

Questions:

OTC - QUESTIONS SECTION

jacksonsnaturals.com or

faq@jacksonsnaturals.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84739-008-01Jacksons Cell Salts KALI SULPH 6X7500 [hp_X] in 1 BOTTLEPELLET5001
84739-008-01Jacksons Cell Salts KALI SULPH 6X71 in 1 CARTONPELLET11

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84739-00884739-008-01

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
NameUNIIKind
POTASSIUM SULFATE1K573LC5TVACTIB
SUCROSEC151H8M554IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Jacksons Cell Salts KALI SULPH 6X 7KALI SULPHURICUMZettl Health Inc.36b13bb9-c3f9-adc5-e063-6394a90af2472025-06-03WarningsExact identifier
ndc (package): 84739-008-01
ndc (product): 84739-008
ndc11 (package): 84739000801
spl id: 36b13bb9-c3fa-adc5-e063-6394a90af247
spl set id: 36b13bb9-c3f9-adc5-e063-6394a90af247

Reported adverse events (FAERS/openFDA)#

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