Magsoothium CBD Body Spray

Manufacturer
Ubu/Elements, Inc.
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:25:48

Label at a glance#

ProductMagsoothium CBD Body
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Menthol USP 5.0%

Purpose

Pain Reliever

OTC - PURPOSE SECTION

Uses: Temporarily relieves minor aches and pains associated with

  • sore muscles and joints
  • arthritis
  • backache
  • muscle strains
  • sprains
  • bruises

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE SECTION

Stop use and ask a doctor if: Condition worsens or symptoms persist for more than 7 days or clear up and recur

  • Redness is present or irritation develops

WARNINGS SECTION

Warnings: For external use only

When using this product: use only as directed

Do not bandage or cover the area being treated
Do not apply ice or heating pad in conjunction with this product

Do not use with any medical device or other device

Do not combine with any other topical treatment

Avoid contact with eyes or mucous membrane

Do not apply to wounds or damaged skin

If pregnant or breast-feeding: Ask a health professional before use

DOSAGE & ADMINISTRATION SECTION

Directions: Adults and children over the age of 2 years old:

Apply generously with gentle rubbing to the affected area 2-3 times daily or as needed

Children less than 2 years of age: Consult a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, PEG-40 Hydrogenated Castor Oil, Magnesium Sulfate Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Arnica Montana Flower Extract, Phenoxyethanol, Sodium Benzoate, Ethylhexylglycerin, Mentha Piperita (Peppermint) Oil, Potassium Sorbate, Aloe Barbadensis Leaf Extract, Citric Acid, Propanediol, Polysorbate 20, 1,2-Hexanediol, Caprylhydroxamic Acid, Glycerin, Argania Spinosa Kernel Oil, Prunus Armeniaca (Apricot) Kernel Oil, Olea Europaea (Olive) Fruit Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Lobelia inflata Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Magsoothium Body Spray

Helps Relieve Minor Aches & Pains

Homeopathic Pain Reliever

magnesium & arnica based formula

Net Contents: 4 fl oz. (118.3ml)

Made in U.S.A

spray labelspray label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128883774100394VEGE LAB 4 oz spray label-.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83262-004-01Magsoothium CBD Body118 mL in 1 BOTTLESPRAY1183

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83262-00483262-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
Magsoothium CBD BodyMENTHOLUbu/Elements, Inc.00b2ef34-42d7-523c-e063-6294a90a753d2025-12-16WarningsExact identifier
ndc (package): 83262-004-01
ndc (product): 83262-004
ndc11 (package): 83262000401
spl id: 4615f436-a473-9178-e063-6394a90a70e9
spl set id: 00b2ef34-42d7-523c-e063-6294a90a753d

Reported adverse events (FAERS/openFDA)#

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