FDA.reportPublic FDA data

Jacksons Cell Salts KALI PHOS 6X

Manufacturer
Zettl Health Inc.
Effective date
2025-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:33:30

Label at a glance#

ProductJacksons Cell Salts KALI PHOS 6X 10
Active ingredientPOTASSIUM PHOSPHATE, DIBASIC
Label structure12 sections

Indications and uses

Temporarily relieves: • simple nervous tension

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 phosphoricum 6X

Purpose

OTC - PURPOSE SECTION

Kali phosphoricum - Simple nervous tension

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves:

• simple nervous tension

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
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84739-007-01Jacksons Cell Salts KALI PHOS 6X10500 [hp_X] in 1 BOTTLEPELLET5001
84739-007-01Jacksons Cell Salts KALI PHOS 6X101 in 1 CARTONPELLET11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84739-007JACKSONS CELL SALTS KALI PHOS 6X 10 (KALI PHOSPHORICUM) PELLET [ZETTL HEALTH INC.]1Current NDC, 2 package rows20250507_3467dac6-887e-3677-e063-6294a90a21bb.zip

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
84739-00784739-007-01

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 PHOSPHATE, DIBASICCI71S98N1ZACTIB
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 PHOS 6X 10KALI PHOSPHORICUMZettl Health Inc.3467dac6-887e-3677-e063-6294a90a21bb2025-05-05WarningsExact identifier
ndc (package): 84739-007-01
ndc (product): 84739-007
ndc11 (package): 84739000701
spl id: 3467dac6-887f-3677-e063-6294a90a21bb
spl set id: 3467dac6-887e-3677-e063-6294a90a21bb

Reported adverse events (FAERS/openFDA)#

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