FDA.reportPublic FDA data

Musco MXT

Manufacturer
Sandco International, Inc | Apotheca Company
Effective date
2025-04-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:33:12

Label at a glance#

ProductMusco MXT
Active ingredientPANAX QUINQUEFOLIUS WHOLE, EPIFAGUS VIRGINIANA WHOLE, JACARANDA CAROBA FLOWER, LACTIC ACID, DL-, CENTELLA ASIATICA WHOLE, HYDROGEN CYANIDE
Label structure9 sections

Indications and uses

May temporarily relieve of muscle weakness, muscular pain and stiffness, joint pain and swelling, muscle cramps, spasms, and overall muscle fatigue.

Dosage and administration

Adults Take 10-20 drops under the tongue once twice daily on an empty stomach. Consult a Physician  for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Aralia Quinquefolia 15C HPUS, Epiphegus Virginiana 15C HPUS, Hydrocotyle Asiatica 100C HPUS, Hydrocyanicum Acidum 100C HPUS, Jacaranda Caroba 15C HPUS, Lacticum Acidum 15C HPUS.

PURPOSE:

OTC - PURPOSE SECTION

Aralia Quinquefolia – Fatigue, muscular pain, and stiffness,* Epiphegus Virginiana – Headache related to stress and fatigue,* Hydrocotyle Asiatica - Circulation,* Hydrocyanicum Acidum – Spasms and muscle cramps,* Jacaranda Caroba – Joint pain and swelling,* Lacticum Acidum – Muscle cramp, spasms, and overall muscle fatigue*
*Claims based on traditional homeopathic practice not accepted medical evidence. Not FDA evaluated.

USES:

INDICATIONS & USAGE SECTION

  • May temporarily relieve of muscle weakness, muscular pain and stiffness, joint pain and swelling, muscle cramps, spasms, and overall muscle fatigue.

WARNINGS:

WARNINGS SECTION

Use only as directed.

Stop use and ask doctor if symptoms worsen or do not improve after 5 days.

If pregnant or breast-feeding, consult 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.  

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken. Store in a cool, dry area.

KEEP OUT OF REACH OR CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • Adults Take 10-20 drops under the tongue once twice daily on an empty stomach.
  • Consult a Physician for use in children under 12 years of age.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

20% Ethanol, Purified Water.

QUESTIONS:

OTC - QUESTIONS SECTION

Manufactured for:

SANDCO International, Inc.

Northport, AL 35473

1-800-367-9599

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Homeopathic 

NDC#49892-0002-1

MUSCO MXT

1 FL. OZ (29.6 ml)

Musco MXTMusco MXT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49892-0002-1Musco MXT30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49892-0002MUSCO MXT (ARALIA QUINQUEFOLIA, EPIPHEGUS VIRGINIANA, JACARANDA CAROBA, LACTICUM ACIDUM, HYDROCOTYLE ASIATICA, HYDROCYANICUM ACIDUM,) LIQUID [SANDCO INTERNATIONAL, INC]3Current NDC, Legacy NDC, 1 package rows20250410_c35475c2-b138-4a4e-8e54-9cef93199b45.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CENTELLA ASIATICAACTIVE INGREDIENT7M867G6T1U1
EPIFAGUS VIRGINIANAACTIVE INGREDIENT69J42KMV8D1
HYDROGEN CYANIDEACTIVE INGREDIENT2WTB3V159F1
JACARANDA CAROBA FLOWERACTIVE INGREDIENT0JTX26L7CL1
LACTIC ACID, DL-ACTIVE INGREDIENT3B8D35Y7S41
PANAX QUINQUEFOLIUS WHOLEACTIVE INGREDIENT0P067WOA1X1
CENTELLA ASIATICAACTIVE MOIETY7M867G6T1U1
EPIFAGUS VIRGINIANAACTIVE MOIETY69J42KMV8D1
HYDROGEN CYANIDEACTIVE MOIETY2WTB3V159F1
JACARANDA CAROBA FLOWERACTIVE MOIETY0JTX26L7CL1
LACTIC ACID, DL-ACTIVE MOIETY3B8D35Y7S41
PANAX QUINQUEFOLIUS WHOLEACTIVE MOIETY0P067WOA1X1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49892-000249892-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PANAX QUINQUEFOLIUS WHOLE0P067WOA1XACTIB
EPIFAGUS VIRGINIANA WHOLE69J42KMV8DACTIB
JACARANDA CAROBA FLOWER0JTX26L7CLACTIB
LACTIC ACID, DL-3B8D35Y7S4ACTIB
CENTELLA ASIATICA WHOLE7M867G6T1UACTIB
HYDROGEN CYANIDE2WTB3V159FACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 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
Musco MXTARALIA QUINQUEFOLIA, EPIPHEGUS VIRGINIANA, JACARANDA CAROBA, LACTICUM ACIDUM, HYDROCOTYLE ASIATICA, HYDROCYANICUM ACIDUM,Sandco International, Incc35475c2-b138-4a4e-8e54-9cef93199b452025-04-08WarningsExact identifier
ndc (package): 49892-0002-1
ndc (product): 49892-0002
ndc11 (package): 49892000201
spl id: ba718254-f53b-4e52-b6b8-8c9dc816c1db
spl set id: c35475c2-b138-4a4e-8e54-9cef93199b45

Reported adverse events (FAERS/openFDA)#

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