FDA.reportPublic FDA data

DRUG FACTS:

Manufacturer
The Magni Company | Apotheca Company
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:38:23

Label at a glance#

ProductLeg and Back Pain Relief
Active ingredientCAPSICUM, CITRULLUS COLOCYNTHIS FRUIT PULP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
Label structure10 sections

Indications and uses

For the temporary relief of minor aches and pains in the lower back, buttocks, and legs

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, 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

(in each tablet) Capsicum Annuum 6X HPUS, Colocynthis 6X HPUS, Gnaphalium Polycephalum 6X HPUS, Magnesia Phosphorica 6X HPUS.

PURPOSE:

OTC - PURPOSE SECTION

Capsicum Annuum – For pain from hips to feet, Colocynthis – For pain from hip to knee; for leg pain, Gnaphalium Polycephalum – pain reliever, Magnesia Phosphorica – For lower back pain

USES:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains in the lower back, buttocks, and legs

WARNINGS:

WARNINGS SECTION

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

• Keep out of reach of children 

• Do not take this product for pain for more than 7 days unless directed by a doctor.

• If pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a       serious condition.

• In case of overdose, get medical help or contact a Poison Control Center right away

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

OTHER INFORMATION:

OTHER SAFETY INFORMATION

• Store tightly closed in a dry place

• Tamper Sealed: Sealed for your protection. Do not use if seal is broken or missing

• The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United

   States

• These statements are supported by the traditional homeopathic principles

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, Consult a physician

• Take at least 10 minutes before or after eating or drinking

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Lactose, Magnesium Stearate, Microcrystalline Cellulose

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MAGNILIFE 

LEG & BACK

PAIN RELIEF TABLETS

For relief of sciatica pain symptoms

RELIEVES

• Burning     • Stabbing

• Tingling    • Aching

Homeopathic NDC: 43689-0013-1

125 Dissolving Tablets

Leg and Back Pain Relief LBLLeg and Back Pain Relief LBL

Leg and Back Pain Relief CTNLeg and Back Pain Relief CTN

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43689-0013-1Leg and Back Pain Relief125 in 1 BOTTLETABLET1254
43689-0013-2Leg and Back Pain Relief1 in 1 CARTONTABLET14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAPSICUMACTIVE INGREDIENT00UK7646FG1
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE INGREDIENT23H32AOH171
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEACTIVE INGREDIENTHF539G9L3Q1
PSEUDOGNAPHALIUM OBTUSIFOLIUMACTIVE INGREDIENT36XQ854NWW1
CAPSICUMACTIVE MOIETY00UK7646FG1
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE MOIETY23H32AOH171
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY8381
PSEUDOGNAPHALIUM OBTUSIFOLIUMACTIVE MOIETY36XQ854NWW1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43689-001343689-0013-1, 43689-0013-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPSICUM00UK7646FGACTIB
CITRULLUS COLOCYNTHIS FRUIT PULP23H32AOH17ACTIB
PSEUDOGNAPHALIUM OBTUSIFOLIUM36XQ854NWWACTIB
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATEHF539G9L3QACTIB
LACTOSEJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / ORAL2500 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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
Leg and Back Pain ReliefCAPSICUM ANNUUM, COLOCYNTHIS, GNAPHALIUM POLYCEPHALUM, MAGNESIA PHOSPHORICAThe Magni Companyef30c7cf-6da0-424d-8737-c968436768fd2026-04-22WarningsExact identifier
ndc (package): 43689-0013-2
ndc (package): 43689-0013-1
ndc (product): 43689-0013
ndc11 (package): 43689001301
ndc11 (package): 43689001302
spl id: bc3ebce9-dde9-4bde-8568-878ab1c5be26
spl set id: ef30c7cf-6da0-424d-8737-c968436768fd

Reported adverse events (FAERS/openFDA)#

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