Natrum Phosphoricum

Manufacturer
Ratis, LLC
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:15:37

Label at a glance#

ProductNatrum Phosphoricum
Active ingredientSODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Label structure9 sections

Indications and uses

Helps relieve heartburn, belching, indigestion, gas, diarrhea, and baby colic. Alleviates rheumatic conditions and joint pain. Establishes a healthy pH balance.** **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Dosage and administration

Adults: 2 sprays 3 times a day or as needed. Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT:

OTC - ACTIVE INGREDIENT SECTION

Natrum Phosphoricum 6X.

USES:

OTC - PURPOSE SECTION

Helps relieve heartburn, belching, indigestion, gas, diarrhea, and baby colic. Alleviates rheumatic conditions and joint pain. Establishes a healthy pH balance.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

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

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults: 2 sprays 3 times a day or as needed.

Children 2-12: 1 spray as above. For children 12 and under, consult a doctor.

INDICATIONS:

INDICATIONS & USAGE SECTION

Helps relieve heartburn, belching, indigestion, gas, diarrhea, and baby colic. Alleviates rheumatic conditions and joint pain. Establishes a healthy pH balance.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, Organic Ethanol 20%

QUESTIONS:

OTC - QUESTIONS SECTION

Comments? Visit

HomeopathyStore.com

or call (888) 405-7551.

Distributed by:

Ratis, LLC,

211 E. Lombard St, STE 303,

Baltimore, MD 21202

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71753-8010-1

LACTOSE FREE

Anna's

REMEDIES

Natrum Phosphoricum

HOMEOPATHIC ORAL SPRAY

1 FL. OZ (30ML)

Natrum PhosphoricumNatrum Phosphoricum

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-8010NATRUM PHOSPHORICUM SPRAY [RATIS, LLC]2Legacy NDC20220121_3b808bfc-551a-4561-ab11-2f91e030aef7.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
71753-801071753-8010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
f8f8d698-66d8-409e-a9f9-38118cb3fc7a3b808bfc-551a-4561-ab11-2f91e030aef72022-01-20WarningsExact identifier
spl id: f8f8d698-66d8-409e-a9f9-38118cb3fc7a
spl set id: 3b808bfc-551a-4561-ab11-2f91e030aef7

Reported adverse events (FAERS/openFDA)#

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