Muscle Cramp Pain Reliever

Manufacturer
The Magni Company | Apotheca Company
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:49

Label at a glance#

ProductMuscle Cramp Pain Reliever
Active ingredientCAUSTICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, COPPER, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, PHYTOLACCA AMERICANA ROOT, TOXICODENDRON PUBESCENS LEAF, TIN, VERATRUM ALBUM ROOT
Label structure9 sections

Indications and uses

Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, hips and back.

Dosage and administration

Adults and children 12 years and above, dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician. Children under 12 years of age, consult a physician. Take at least 10 minutes before or after eating or drinking.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album

INDICATIONS

OTC - PURPOSE SECTION

Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, feet, hips and back.

WARNINGS

WARNINGS SECTION

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Is symptoms persist for more than 7 days or worsens, consult your physician.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away. If symptoms persist for more than 7 days or worsens, consult your physician.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and above, dissolve 2 tablets under tongue 2 to 3 times daily or as directed by a physician.

Children under 12 years of age, consult a physician. Take at least 10 minutes before or after eating or drinking.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, hips and back.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

QUESTIONS

OTC - QUESTIONS SECTION

Dist. by:

The Magni Group, Inc. McKinney, TX 75071 USA

www.magnilife.com 1-800-645-9199

PACKAGE LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAGNILIFE

Homeopathic

NDC 43689-0022-1

MUSCLE CRAMP PAIN RELIEVER

For relief of muscle pain, cramping and stiffness,

√Legs

√Feet

√Back

√Hips

√Joints

125 Dissolving Tablets

Muscle Cramp Pain Reliever lblMuscle Cramp Pain Reliever lbl

Muscle Cramp Pain Reliever ctnMuscle Cramp Pain Reliever ctn

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
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
43689-0022-22024-11-05C16284748780-1ba0f9c33-2875-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0022-22024-01-30C16284748780-1ba0f9c33-2875-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0022-22022-01-10C16284748780-1ba0f9c33-2875-a910-e053-dadaa90a0b85DRUG FACTS:
43689-0022-22021-01-29C16284748780-1ba0f9c33-2875-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0022-1Muscle Cramp Pain Reliever125 in 1 BOTTLETABLET1253
43689-0022-2Muscle Cramp Pain Reliever1 in 1 CARTONTABLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43689-0022MUSCLE CRAMP PAIN RELIEVER (CAUSTICUM, COLOCYNTHIS, CUPRUM METALLICUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RHUS TOX, STANNUM METALLICUM, VERATRUM ALBUM) TABLET [THE MAGNI COMPANY]3Current NDC, Legacy NDC, 2 package rows20241107_e8d70c35-3ed6-479a-8213-b2fb3499a32a.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-002243689-0022-1, 43689-0022-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Muscle Cramp Pain RelieverCAUSTICUM, COLOCYNTHIS, CUPRUM METALLICUM, MAGNESIA PHOSPHORICA, PHYTOLACCA DECANDRA, RHUS TOX, STANNUM METALLICUM, VERATRUM ALBUMThe Magni Companye8d70c35-3ed6-479a-8213-b2fb3499a32a2024-11-05WarningsExact identifier
ndc (package): 43689-0022-1
ndc (package): 43689-0022-2
ndc (product): 43689-0022
ndc11 (package): 43689002201
ndc11 (package): 43689002202
spl id: b7218efa-ddaa-4879-998f-4fd35196c21c
spl set id: e8d70c35-3ed6-479a-8213-b2fb3499a32a

Reported adverse events (FAERS/openFDA)#

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