MAGNESIA PHOS

Manufacturer
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Effective date
2024-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:27:19

Label at a glance#

ProductMAGNESIA PHOS
Active ingredientMAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Label structure9 sections

Indications and uses

USES: Temporary Relief - Running Colic * * Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Storage and handling

Store in a cool dark place

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

MAGNESIA PHOS HPUS 1X and higher

USES

OTC - PURPOSE SECTION

USES: Temporary Relief - Running Colic *

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

INDICATIONS

INDICATIONS & USAGE SECTION

Condition listed above or as directed by the physician

DOSAGE

DOSAGE & ADMINISTRATION SECTION

Adults: Mix 4-6 drops in 1/2 cup of water, take orally three times daily or as directed by a physician. Children (2 years and older): Take half 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

Active: As Above; Inactive: ENA 50% v/v and Purified Water q.s.

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 2940 Eisenhower St., Suite 100, Carrollton, TX 75007 USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Carton BoxCarton Box

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
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11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
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86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
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290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
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c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2833-0MAGNESIA PHOS10 mL in 1 BOTTLELIQUID101
15631-2833-1MAGNESIA PHOS30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2833MAGNESIA PHOS LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240612_19cf2bbd-0f15-78a7-e063-6394a90a1647.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
15631-283315631-2833-0, 15631-2833-1

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
MAGNESIA PHOSMAGNESIA PHOSRxhomeo Private Limited d.b.a. Rxhomeo, Inc19cf2bbd-0f15-78a7-e063-6394a90a16472024-06-01WarningsExact identifier
ndc (package): 15631-2833-0
ndc (package): 15631-2833-1
ndc (product): 15631-2833
ndc11 (package): 15631283300
ndc11 (package): 15631283301
spl id: 19cf3431-37ee-dcf8-e063-6394a90ae7d3
spl set id: 19cf2bbd-0f15-78a7-e063-6394a90a1647

Reported adverse events (FAERS/openFDA)#

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