FDA.reportPublic FDA data

Natrum Mur

Manufacturer
Warsan Homoeopathic Laboratories
Effective date
2017-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:12:05

Label at a glance#

ProductNatrum Mur
Active ingredientSODIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Natrum Muriaticum 12X (HPUS)

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INACTIVE INGREDIENT SECTION

Lactose.

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 - PURPOSE SECTION

Temporary relief from sneezing, cold, hayfever, hives.

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.

INDICATIONS & USAGE SECTION

Temporary relief from sneezing, cold, hayfever, hives.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

natrum mur 12x.jpgnatrum mur 12x.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69008-0026-12020-08-17C16284748780-19d75b9d0-e3d1-f424-e053-dadaa90a57ce5966babe-bb24-4ef1-e053-2991aa0ae8c5
69008-0026-12020-01-31C16284748780-19d75b9d0-e3d1-f424-e053-dadaa90a57ce5966babe-bb24-4ef1-e053-2991aa0ae8c5

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
69008-002669008-0026-1

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
NameUNIIKind
LACTOSEJ2B2A4N98GIACT
SODIUM CHLORIDE451W47IQ8XACTIB

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
ad15ade2-5dcc-9151-e053-2a95a90ac5fd5966babe-bb24-4ef1-e053-2991aa0ae8c52020-08-17WarningsExact identifier
spl set id: 5966babe-bb24-4ef1-e053-2991aa0ae8c5

Reported adverse events (FAERS/openFDA)#

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