Natrum Sulph

Manufacturer: Warsan Homoeopathic Laboratories
Effective date: 2018-06-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:54:27

Label at a glance#

ProductNatrum Sulph

Active ingredientSODIUM SULFATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

WARNINGS SECTION

Stop use and ask doctor if symptoms worsen or persist longer than 7 days.

If pregnant or breast-feeding, ask health professional before use.

OTC - ACTIVE INGREDIENT SECTION

Natrum Sulphuricum 6X (HPUS)

OTC - PURPOSE SECTION

Temporary relief from congestion headache, nasal discharge.

INACTIVE INGREDIENT SECTION

Lactose.

INDICATIONS & USAGE SECTION

Temporary relief from congestion headache, nasal discharge.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older: Four tablets every thirty minutes for six doses followed by four tablets every 4-6 hours as needed.

Children 2 years to under 12 years: Four tablets every thirty minutes for six doses followed by two tablets every 4-6 hours as needed.

Children under 2 years age: Consult doctor prior to use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

natrum sulph 6x 1031.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69008-1031-1	2020-08-17	C162847	48780-1	9d75b9d0-ab28-f424-e053-dadaa90a57ce	6edefce7-e2b1-8a17-e053-2a91aa0a02d0
69008-1031-1	2020-01-31	C162847	48780-1	9d75b9d0-ab28-f424-e053-dadaa90a57ce	6edefce7-e2b1-8a17-e053-2a91aa0a02d0

Products#

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

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

Natrum Sulph
Natrum Sulphuricum
LACTOSE
SODIUM SULFATE
SODIUM SULFATE ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69008-1031	69008-1031-1

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
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
SODIUM SULFATE	0YPR65R21J	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ad164b72-7b6a-4e81-e053-2a95a90a2de2			6edefce7-e2b1-8a17-e053-2a91aa0a02d0	2020-08-17	Warnings	Exact identifier spl set id: 6edefce7-e2b1-8a17-e053-2a91aa0a02d0

Reported adverse events (FAERS/openFDA)#

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