FDA.reportPublic FDA data

Magnesia Phosphorica

Manufacturer
SEVENE USA
Effective date
2025-02-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:32:07

Label at a glance#

ProductMagnesia Phosphorica 6X
Active ingredientMAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Label structure11 sections

Indications and uses

Cramps, muscle pain, and nervous tissues**.

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

Magnesia Phosphorica 6X**.

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

TRADITIONALLY USE FOR TEMPORARY RELIEF FROM:

OTC - PURPOSE SECTION

Cramps, muscle pain, and nervous tissues*

*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

Cramps, muscle pain, and nervous tissues**.

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_Magnesia Phosphorica_6X_80ct01b LBL_Magnesia Phosphorica_6X_80ct

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76472-4095-12025-02-11C16284748780-12cef2736-947b-d83d-e063-dadaa90ab31fSEVENE USA (as PLD) - Magnesia Phosphorica 6X (76472-4095)
76472-4095-12025-01-30C16284748780-12cef2736-947b-d83d-e063-dadaa90ab31fSEVENE USA (as PLD) - Magnesia Phosphorica 6X (76472-4095)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-4095-1Magnesia Phosphorica6X80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-4095MAGNESIA PHOSPHORICA 6X (MAGNESIA PHOSPHORICA) PELLET [SEVENE USA]4Current NDC, 1 package rows20250213_ff0efbc2-d7a9-9783-e053-6394a90a384f.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
76472-409576472-4095-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEHF539G9L3QACTIB

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
Magnesia Phosphorica 6XMAGNESIA PHOSPHORICASEVENE USAff0efbc2-d7a9-9783-e053-6394a90a384f2025-02-11WarningsExact identifier
ndc (package): 76472-4095-1
ndc (product): 76472-4095
ndc11 (package): 76472409501
spl id: 2ddc5b58-760f-5f6f-e063-6294a90a8984
spl set id: ff0efbc2-d7a9-9783-e053-6394a90a384f

Reported adverse events (FAERS/openFDA)#

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