FDA.reportPublic FDA data

Jacksons Cell Salts CALC 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 CALC SULPH 6X 3
Active ingredientCALCIUM SULFATE ANHYDROUS
Label structure12 sections

Indications and uses

Temporarily relieves: • acne

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

Calcarea sulphurica 6X

Purpose

OTC - PURPOSE SECTION

Calcarea sulphurica -- Acne

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves:

• acne

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
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84739-003-01Jacksons Cell Salts CALC SULPH 6X31 in 1 CARTONPELLET11
84739-003-01Jacksons Cell Salts CALC SULPH 6X3500 [hp_X] in 1 BOTTLEPELLET5001

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
84739-00384739-003-01

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
CALCIUM SULFATE ANHYDROUSE934B3V59HACTIB
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 CALC SULPH 6X 3CALCAREA SULPHURICAZettl Health Inc.36b1104c-0989-7f21-e063-6394a90a0f0c2025-06-03WarningsExact identifier
ndc (package): 84739-003-01
ndc (product): 84739-003
ndc11 (package): 84739000301
spl id: 36b1104c-098a-7f21-e063-6394a90a0f0c
spl set id: 36b1104c-0989-7f21-e063-6394a90a0f0c

Reported adverse events (FAERS/openFDA)#

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