Natrum Sulphuricum

Manufacturer
Ratis, LLC
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:15:37

Label at a glance#

ProductNatrum Sulphuricum
Active ingredientSODIUM SULFATE
Label structure9 sections

Indications and uses

Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

Adults: 2 sprays 3 times a day or as needed. Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Natrum Sulphuricum 6X.

USES:

OTC - PURPOSE SECTION

Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults: 2 sprays 3 times a day or as needed.

Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

INDICATIONS:

INDICATIONS & USAGE SECTION

Helps relieve nausea, vomiting, bitter taste, diarrhea, and influenza. Eliminates toxins and supports liver health.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, Organic Ethanol 20%

QUESTIONS:

OTC - QUESTIONS SECTION

Comments? Visit

HomeopathyStore.com

or call (888) 405-7551.

Distributed by:

Ratis, LLC,

211 E. Lombard St, STE 303,

Baltimore, MD 21202

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71753-8011-1

LACTOSE FREE

Anna's

REMEDIES

NATRUM SULPHURICUM

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

NATRUM SULPHURICUMNATRUM SULPHURICUM

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-8011NATRUM SULPHURICUM SPRAY [RATIS, LLC]2Legacy NDC20220121_ca0e0398-3e97-4e6c-a419-cdfb6f85bce6.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
71753-801171753-8011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM SULFATE0YPR65R21JACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
2cc44cf3-5cfb-4a35-a8ea-06831753548aca0e0398-3e97-4e6c-a419-cdfb6f85bce62022-01-20WarningsExact identifier
spl id: 2cc44cf3-5cfb-4a35-a8ea-06831753548a
spl set id: ca0e0398-3e97-4e6c-a419-cdfb6f85bce6

Reported adverse events (FAERS/openFDA)#

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