FDA.reportPublic FDA data

Natrium Muriaticum 6X

Manufacturer
Seroyal USA | SAN’UP
Effective date
2022-07-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:17:41

Label at a glance#

ProductNatrium Muriaticum 6X
Active ingredientSODIUM CHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Natrum muriaticum (Sodium chloride) 6X

OTC - PURPOSE SECTION

Uses

Helps promote and maintain healthy water balance.

For the temporary relief of symptoms associated with general colds.

WARNINGS SECTION

Warnings

Do not use if you ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist or worsen.

If you are pregnant or breastfeeding, ask a healthcare practitioner before use.
Keep out of reach of children.

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breastfeeding, ask a healthcare practitioner before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact

a Poison Control Center right away.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if symptoms persist or worsen.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Lactose monohydrate (milk), magnesium stearate, sodium carboxymethylcellulose, xylitol

DOSAGE & ADMINISTRATION SECTION

Directions

Tip bottle slightly allowing for tablets to
fall into the cap.
Use cap to drop tablets into mouth and
allow them to dissolve under the tongue.

Adults and adolescents (12 years and older): Take 1 to 4 tablets, one to four times daily,

or as recommended by your healthcare practitioner.

Children (under 12 years): Take under the direction of your healthcare practitioner.

INDICATIONS & USAGE SECTION

Uses

Helps promote and maintain healthy water balance.

For the temporary relief of symptoms associated with general colds.

Directions

Tip bottle slightly allowing tablets to fall into cap.

Use cap to drop tablets into mouth and allow them to dissolve under the tongue.
Adults and adolescents (12 years and older): Take 1 to 4 tablets, one to
four times daily, or as recommended by your healthcare practitioner.

Children (under 12 years): Take under the direction of your healthcare practitioner.

OTHER SAFETY INFORMATION

Other information

Do not use if seal is missing or broken.

Store in a cool, dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 62106-1058-2

UNDA

tissue salt

NATRIUM MURIATICUM 6X

Homeopathic Preparation

Schüessler Salt

Helps promote and maintain healthy water balance and for the temporary relief of symptoms associated with general colds.

100 Tablets

NDC 62106-1058-2NDC 62106-1058-2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1058-2Natrium Muriaticum 6X1 in 1 BOXTABLET15
62106-1058-2Natrium Muriaticum 6X100 in 1 BOTTLE, GLASSTABLET1005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1058NATRIUM MURIATICUM 6X (SODIUM CHLORIDE) TABLET [SEROYAL USA]5Current NDC, Legacy NDC, 2 package rows20220709_0ebf18de-12fe-0bc4-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS3111
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5X1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301
XYLITOLINACTIVE INGREDIENTVCQ006KQ1E1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-105862106-1058-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
XYLITOLVCQ006KQ1EIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
MAGNESIUM STEARATE70097M6I30IACT
SODIUM CHLORIDE451W47IQ8XACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / BUCCAL4 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / ORAL280 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
4 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / ORAL280 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
CARBOXYMETHYLCELLULOSE SODIUMCARBOXYMETHYLCELLULOSE SODIUMK679OBS311TABLET / BUCCAL4 mgExact identifier — unii+dosage form
4 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
Natrium Muriaticum 6XSODIUM CHLORIDESeroyal USA0ebf18de-12fe-0bc4-e054-00144ff88e882022-07-07WarningsExact identifier
ndc (package): 62106-1058-2
ndc (product): 62106-1058
ndc11 (package): 62106105802
spl id: e33d76f2-f4e6-3478-e053-2995a90ac970
spl set id: 0ebf18de-12fe-0bc4-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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