FDA.reportPublic FDA data

Jacksons Cell Salts NAT SULPH 6X

Manufacturer
Zettl Health Inc.
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:11

Label at a glance#

ProductJacksons Cell Salts NAT SULPH 6X 11
Active ingredientSODIUM SULFATE
Label structure12 sections

Indications and uses

Temporarily relieves: • Gas, • Bloating

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Natrum sulphuricum 6X

Purpose

OTC - PURPOSE SECTION

Natrum sulphuricum 6X -- Gas, bloating

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves:

• Gas,

• Bloating

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.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

SPL UNCLASSIFIED SECTION

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

†“HPUS” is the Homeopathic Pharmacopeia of the United States.

Do not use if tamper evident seal broken or missing.

Manufactured in the USA for Jackson's Naturals, a division of Zettl Health Inc., P.O. Box 52238, North Vancouver, BC V7J 3V5 Canada.

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 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
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84739-012-01Jacksons Cell Salts NAT SULPH 6X111 in 1 CARTONPELLET11
84739-012-01Jacksons Cell Salts NAT SULPH 6X11500 [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
84739-01284739-012-01

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
SODIUM SULFATE0YPR65R21JACTIB
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 NAT SULPH 6X 11NATRUM SULPHURICUMZettl Health Inc.41ecb3e5-ae90-839f-e063-6394a90a600c2025-10-24WarningsExact identifier
ndc (package): 84739-012-01
ndc (product): 84739-012
ndc11 (package): 84739001201
spl id: 41ecb3fe-5234-8ae0-e063-6394a90a4e4e
spl set id: 41ecb3e5-ae90-839f-e063-6394a90a600c

Reported adverse events (FAERS/openFDA)#

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