Natrum Phosphoricum

Manufacturer
SEVENE USA
Effective date
2025-02-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:32:06

Label at a glance#

ProductNatrum Phosphoricum 6X
Active ingredientSODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Label structure11 sections

Indications and uses

Indigestion, heartburn, and gas**. **C, K, CK & X are homeopathic dilutions

Dosage and administration

(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Natrum Phosphoricum 6X**.

**C, K, CK & X are homeopathic dilutions.

TRADITIONALLY USE FOR TEMPORARY RELIEF FROM:

OTC - PURPOSE SECTION

Indigestion, heartburn, and gas*

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • (adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.

USES:

INDICATIONS & USAGE SECTION

Indigestion, heartburn, and gas**.

**C, K, CK & X are homeopathic dilutions

WARNINGS:

WARNINGS SECTION

  • Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

  • If pregnant or breast-feeding, ask a health professional prior to use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.
  • In case of overdose, get medical help.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

  • Store at room temperature.
  • Do not use if tamper-evidence seal is broken.
  • Organic verified by Alpes Contrôle 2021/A03M216K/1.

INACTIVE INGREDIENT:

INACTIVE INGREDIENT SECTION

Organic Sucrose.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

Email us at: info@ollois.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Natrum Phosphoricum_6X_80ct01b LBL_Natrum Phosphoricum_6X_80ct

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4097-1Natrum Phosphoricum6X80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4097NATRUM PHOSPHORICUM 6X (NATRUM PHOSPHORICUM) PELLET [SEVENE USA]4Current NDC, 1 package rows20250213_ff0d77ad-3e04-25ea-e053-6294a90a0def.zip

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
76472-409776472-4097-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

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
Natrum Phosphoricum 6XNATRUM PHOSPHORICUMSEVENE USAff0d77ad-3e04-25ea-e053-6294a90a0def2025-02-11WarningsExact identifier
ndc (package): 76472-4097-1
ndc (product): 76472-4097
ndc11 (package): 76472409701
spl id: 2ddc5714-317d-0005-e063-6394a90af292
spl set id: ff0d77ad-3e04-25ea-e053-6294a90a0def

Reported adverse events (FAERS/openFDA)#

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