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: SODIUM CHLORIDE
Manufacturer: Hyland's Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 21ee53eb-b41a-4d2e-8037-12973d2b73d9
SPL ID: f03159cf-dfd9-fdf2-e053-2a95a90a5837
Version: 4
Effective date: 2022-12-19
Source export date: 2026-10-27
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/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:43:38

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		NATRUM MURIATICUM	openfda.brand_name
generic name		SODIUM CHLORIDE	openfda.generic_name
manufacturer name		Hyland's Inc.	openfda.manufacturer_name
ndc	package	54973-6433-2	openfda.package_ndc
ndc	package	54973-6433-1	openfda.package_ndc
ndc	product	54973-6433	openfda.product_ndc
ndc11	package	54973643302	derived:openfda.package_ndc
ndc11	package	54973643301	derived:openfda.package_ndc
spl id		f03159cf-dfd9-fdf2-e053-2a95a90a5837	id
spl set id		21ee53eb-b41a-4d2e-8037-12973d2b73d9	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 Do not use if imprinted cap band is broken or missing. If symptoms persist for more than 7 days or worsen, contact a licensed health care provider. If you are pregnant or nursing, seek the advice of a licensed health care provider before using this product. Keep all medications out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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