FERRUM PHOSPHORICUM 6X

Manufacturer
Seroyal USA | SAN’UP
Effective date
2021-07-14
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 02:14:40

Label at a glance#

ProductNATRIUM SULFURICUM 6X
Active ingredientSODIUM SULFATE, POTASSIUM PHOSPHATE, MONOBASIC, FERROSOFERRIC PHOSPHATE
Label structure35 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Natrium sulfuricum (Sodium sulfate anhydrous) 6X

OTC - PURPOSE SECTION

Uses
For the temporary relief of symptoms associated with mild indigestion.

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 pregnant or breastfeeding, ask a health professional 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 pregnant or breastfeeding, ask a health professional 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.

OTHER SAFETY INFORMATION

Other information
Do not use if seal is missing or broken.
Store in a cool, dry place.

Contents may not fill package in order
to accommodate required labeling.
Please rely on stated quantity.

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 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
For the temporary relief of symptoms associated with mild indigestion.

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 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.

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Kalium phosphoricum (Dibasic potassium phosphate) 6X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with

occasional anxiety
overexertion

mental fatigue

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 pregnant or breastfeeding, ask a health professional 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 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

Indications
For the temporary relief of symptoms associated with

occasional anxiety

overexertion

mental fatigue

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.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Ferrum phosphoricum (Ferrosoferric phosphate) 6X

OTC - PURPOSE SECTION

Uses

For the temporary relief of symptoms associated with fever and minor inflammatory conditions.

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
For the temporary relief of symptoms
associated with fever and minor inflammatory conditions.

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 children (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.

Contents may not fill package in order
to accommodate required labeling.
Please rely on stated quantity.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1060-262106-1060-2

NDC 62106-1060-2

UNDA

tissue salt

NATRIUM SULFURICUM 6X

Homeopathic Remedy

Schuessler salt

For the temporary relief of symptoms
associated with mild indigestion.

100 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1055-262106-1055-2

NDC 62106-1055-2

UNDA
tissue salt
NDC 62106-1055-2
KALIUM PHOSPHORICUM 6X
Homeopathic Remedy
Schuessler salt

For the temporary relief of symptoms
associated with occasional anxiety, overexertion and mental fatigue.

100 Tablets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

62106-1053-262106-1053-2

NDC 62106-1053-2

UNDA
tissue salt
FERRUM PHOSPHORICUM 6X
Homeopathic Remedy
Cell salt
For the temporary relief of symptoms
associated with fever and minor inflammatory conditions.
100 Tablets

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62106-1053-2FERRUM PHOSPHORICUM 6X1 in 1 CARTONTABLET111
62106-1053-2FERRUM PHOSPHORICUM 6X100 in 1 BOTTLE, GLASSTABLET10011
62106-1055-2KALIUM PHOSPHORICUM 6X100 in 1 BOTTLE, GLASSTABLET10011
62106-1055-2KALIUM PHOSPHORICUM 6X1 in 1 CARTONTABLET111
62106-1060-2NATRIUM SULFURICUM 6X1 in 1 CARTONTABLET111
62106-1060-2NATRIUM SULFURICUM 6X100 in 1 BOTTLE, GLASSTABLET10011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62106-1053NATRIUM SULFURICUM 6X (ANHYDROUS SODIUM SULFATE) TABLET KALIUM PHOSPHORICUM 6X (POTASSIUM DIHYDROGEN PHOSPHATE) TABLET FERRUM PHOSPHORICUM 6X (HYDRATED IRON III PHOSPHATE) TABLET [SEROYAL USA]11Current NDC, Legacy NDC, 2 package rows20210715_14f4f926-0742-12cd-e054-00144ff8d46c.zip
62106-1055NATRIUM SULFURICUM 6X (ANHYDROUS SODIUM SULFATE) TABLET KALIUM PHOSPHORICUM 6X (POTASSIUM DIHYDROGEN PHOSPHATE) TABLET FERRUM PHOSPHORICUM 6X (HYDRATED IRON III PHOSPHATE) TABLET [SEROYAL USA]11Current NDC, Legacy NDC, 2 package rows20210715_14f4f926-0742-12cd-e054-00144ff8d46c.zip
62106-1060NATRIUM SULFURICUM 6X (ANHYDROUS SODIUM SULFATE) TABLET KALIUM PHOSPHORICUM 6X (POTASSIUM DIHYDROGEN PHOSPHATE) TABLET FERRUM PHOSPHORICUM 6X (HYDRATED IRON III PHOSPHATE) TABLET [SEROYAL USA]11Current NDC, Legacy NDC, 2 package rows20210715_14f4f926-0742-12cd-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FERROSOFERRIC PHOSPHATEACTIVE INGREDIENT91GQH8I5F76
POTASSIUM PHOSPHATE, MONOBASICACTIVE INGREDIENT4J9FJ0HL516
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21J6
FERROSOFERRIC PHOSPHATEACTIVE MOIETY91GQH8I5F76
PHOSPHATE IONACTIVE MOIETYNK08V8K8HR6
SODIUM SULFATE ANHYDROUSACTIVE MOIETY36KCS0R7506
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH486
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5X6
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I306
XYLITOLINACTIVE INGREDIENTVCQ006KQ1E6

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62106-105362106-1053-2
62106-105562106-1055-2
62106-106062106-1060-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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 · 30 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
LACTOSE MONOHYDRATELACTOSE MONOHYDRATEEWQ57Q8I5XTABLET / SUBLINGUAL505 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / SUBLINGUAL17.5 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET / SUBLINGUAL10 mgExact identifier — unii+route+dosage form
6 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ESPRAY / SUBLINGUAL22 mgExact identifier — unii+route
12 equally ranked IID candidates
XYLITOLXYLITOLVCQ006KQ1ETABLET / ORAL15.04 mgExact identifier — unii+dosage form
12 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
FERRUM PHOSPHORICUM 6XHYDRATED IRON III PHOSPHATESeroyal USA14f4f926-0742-12cd-e054-00144ff8d46c2021-07-14WarningsExact identifier
ndc (package): 62106-1055-2
ndc (package): 62106-1053-2
ndc (package): 62106-1060-2
ndc (product): 62106-1055
ndc (product): 62106-1060
ndc (product): 62106-1053
ndc11 (package): 62106105502
ndc11 (package): 62106105302
ndc11 (package): 62106106002
spl id: c71d36c4-a11b-62e4-e053-2a95a90ab58a
spl set id: 14f4f926-0742-12cd-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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