FDA.reportPublic FDA data

MUSE APOTHECARY HEMP RITUAL ROLL ON

Manufacturer
LAB-CLEAN, INC
Effective date
2022-04-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:02:28

Label at a glance#

ProductMUSE APOTHECARY HEMP RITUAL ROLL ON
Active ingredientEUCALYPTUS GLOBULUS LEAF, MENTHOL
Label structure6 sections

Indications and uses

Helps relax and recover tensed-up or sore muscles post-workout / also ideal for general daily use for therapeutic relief on the body / the combination of active ingredients helps soothe and moisturize the skin.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Eucalyptus Globulus 2%

Menthol 2%

Purpose

OTC - PURPOSE SECTION

Eucalyptus Globulus (Cooling Relief), Menthol (Muscle Recovery)

Uses

INDICATIONS & USAGE SECTION

Helps relax and recover tensed-up or sore muscles post-workout / also ideal for general daily use for therapeutic relief on the body / the combination of active ingredients helps soothe and moisturize the skin.

Direction

DOSAGE & ADMINISTRATION SECTION

SHAKE WELL BEFORE USE

Apply as needed on the affected area to relieve muscle tension. Rub with hand post application to help product seep into skin. Daily use

Warnings

WARNINGS SECTION

  • External use only
  • Ask a doctor prior to use if you: have sensitive skin, are pregnant or breast feeding, or plan to use on children under 2 years old 
  • Do not get in eyes, wounds or damaged skin.
  • Stop immediately if condition worsens and consult with doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sunflower Oil, Glycerine, Hemp Seed Oil, Emulsifier, Phenoxyethanol, Ethylhexylglycerine 

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
73126-03773126-037-01

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
WATER059QF0KO0RIACT
SUNFLOWER OIL3W1JG795YIIACT
GLYCERINPDC6A3C0OXIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6ACTIB
MENTHOLL7T10EIP3AACTIB

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
dd943c17-9ed7-e1ba-e053-2a95a90a684c4e904464-6c2d-47ae-a8ca-35bd009f98622022-04-26WarningsExact identifier
spl id: dd943c17-9ed7-e1ba-e053-2a95a90a684c
spl set id: 4e904464-6c2d-47ae-a8ca-35bd009f9862

Reported adverse events (FAERS/openFDA)#

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