FDA.reportPublic FDA data

MAGNESIA SULPHURICA

Manufacturer
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | Rxhomeo, Inc
Effective date
2015-12-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:02

Label at a glance#

ProductMAGNESIA SULPHURICA
Active ingredientMAGNESIUM SULFATE HEPTAHYDRATE
Label structure9 sections

Indications and uses

Urethritis

Storage and handling

Store in a cool dark place

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

MAGNESIA SULPHURICA HPUS 1X and Higher

USES

OTC - PURPOSE SECTION

Urethritis

INDICATIONS

INDICATIONS & USAGE SECTION

Condition listed above or as directed by the physician

DOSAGE

DOSAGE & ADMINISTRATION SECTION

Adults- Take 4 or 6 Tablets by mouth, three times daily or as suggested by physician. Children 2 years and older- take 1/2 the adult dose.

WARNINGS

WARNINGS SECTION

This product is to be used for self-limiting conditions

OTC - STOP USE SECTION

If symptoms do not improve in 4 days, or worsen, discontinue use and seek assistance of health professional

OTC - PREGNANCY OR BREAST FEEDING SECTION

As with any drug, if you are pregnant, or nursing a baby, seek professional advice before taking this product

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of reach of children

OTC - DO NOT USE SECTION

Do not use if capseal is broken or missing.

Close the cap tightly after use.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Lactose

STORAGE

STORAGE AND HANDLING SECTION

Store in a cool dark place

QUESTIONS OR COMMENTS

OTC - QUESTIONS SECTION

www.Rxhomeo.com | 1.888.2796642 | info@rxhomeo.com

Rxhomeo, Inc 9415 Burnet Road, Suite 312, Austin, TX 78758

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPL UNCLASSIFIED SECTION

image descriptionimage description

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
15631-0631-02020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-12020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-22020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-32020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-42020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-52020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-62020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b
15631-0631-72020-01-31C16284748780-19d75b9d0-545b-f424-e053-dadaa90a57ce14a3696b-9a88-4ea5-8357-d98356c14d7b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0631-0MAGNESIA SULPHURICA1 in 1 BLISTER PACKTABLET11
15631-0631-1MAGNESIA SULPHURICA4 in 1 BLISTER PACKTABLET41
15631-0631-2MAGNESIA SULPHURICA50 in 1 CONTAINERTABLET501
15631-0631-3MAGNESIA SULPHURICA100 in 1 CONTAINERTABLET1001
15631-0631-4MAGNESIA SULPHURICA250 in 1 CONTAINERTABLET2501
15631-0631-5MAGNESIA SULPHURICA500 in 1 CONTAINERTABLET5001
15631-0631-6MAGNESIA SULPHURICA1000 in 1 CONTAINERTABLET10001
15631-0631-7MAGNESIA SULPHURICA10000 in 1 CONTAINERTABLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0631MAGNESIA SULPHURICA TABLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Legacy NDC, 8 package rows20151229_14a3696b-9a88-4ea5-8357-d98356c14d7b.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
15631-063115631-0631-0, 15631-0631-1, 15631-0631-2, 15631-0631-3, 15631-0631-4, 15631-0631-5, 15631-0631-6, 15631-0631-7

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
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
LACTOSEJ2B2A4N98GIACT

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
2a322647-663f-4204-b312-9a77f1f9d8c314a3696b-9a88-4ea5-8357-d98356c14d7b2015-12-26WarningsExact identifier
spl id: 2a322647-663f-4204-b312-9a77f1f9d8c3
spl set id: 14a3696b-9a88-4ea5-8357-d98356c14d7b

Reported adverse events (FAERS/openFDA)#

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