NATRUM MURIATICUM

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: NATRUM MURIATICUM
Generic name: NATRUM MURIATICUM
Manufacturer: Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 520edb18-5f2a-4448-ba53-83408a839e1f
SPL ID: ca51bc44-0045-ff83-e053-2a95a90adb8c
Version: 4
Effective date: 2021-09-02
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:13:06

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		NATRUM MURIATICUM	openfda.brand_name
generic name		NATRUM MURIATICUM	openfda.generic_name
manufacturer name		Rxhomeo Private Limited d.b.a. Rxhomeo, Inc	openfda.manufacturer_name
ndc	package	15631-0309-7	openfda.package_ndc
ndc	package	15631-0309-3	openfda.package_ndc
ndc	package	15631-0309-6	openfda.package_ndc
ndc	package	15631-0309-1	openfda.package_ndc
ndc	package	15631-0309-5	openfda.package_ndc
ndc	package	15631-0309-2	openfda.package_ndc
ndc	package	15631-0309-4	openfda.package_ndc
ndc	package	15631-0309-0	openfda.package_ndc
ndc	product	15631-0309	openfda.product_ndc
ndc11	package	15631030905	derived:openfda.package_ndc
ndc11	package	15631030907	derived:openfda.package_ndc
ndc11	package	15631030902	derived:openfda.package_ndc
ndc11	package	15631030903	derived:openfda.package_ndc
ndc11	package	15631030900	derived:openfda.package_ndc
ndc11	package	15631030901	derived:openfda.package_ndc
ndc11	package	15631030906	derived:openfda.package_ndc
ndc11	package	15631030904	derived:openfda.package_ndc
spl id		ca51bc44-0045-ff83-e053-2a95a90adb8c	id
spl set id		520edb18-5f2a-4448-ba53-83408a839e1f	set_id
unii		451W47IQ8X	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS This product is to be used for self-limiting conditions If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional As with any drug, if you are preganant, or nursing a baby, seek professional advice before taking this product Keep this and all medication out of reach of children

Reported adverse events (FAERS/openFDA)#

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