Magsoothium Body Cream Cooling Formula

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 01:26:00

Label at a glance#

ProductMagsoothium Body Cooling Formula
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol USP 5.0%

Purpose
Topical Analgesic

OTC - PURPOSE SECTION

Uses Temporary 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 2 years of age and older

Apply directly onto affected area without the need to rub, massage or bandage

  • repeat as necessary but do not apply more than 4 times daily

Children under 2 years of age Consult a physician

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water, Cocos Nucifera (Coconut) Oil, Cannabis Sativa Seed Oil, Olea Europaea (Olive) Fruit Oil, Glyceryl Stearate, Glycerin, Polyglyceryl-2 Stearate, PEG-100 Stearate, Cetearyl Acohol, Mangifera indica (Mango) Seed Butter, Stearyl Alcohol, Magnesium Sulfate, Mentha Piperita (Peppermint) Oil, Alcohol Denat., Phenoxyethanol,

Ethylhexylglycerin, Xanthan Gum, Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Arnica Montana Flower Extract, Magnesium Chloride, Polysorbate 60

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Homeopathic Pain Reliever

Magsoothium CBD Cooling Formula

Magsoothium Body Cream

Helps relieve minor aches & pains

Net Contents: 4 oz (112 ml)

Cooling JarCooling Jar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83262-002-01Magsoothium Body Cooling Formula112 mL in 1 JARCREAM1123

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
83262-00283262-002-01

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 Body Cooling FormulaMENTHOLUbu/Elements, Inc.f7fb6ac9-a920-a440-e053-6394a90aaa352025-12-16WarningsExact identifier
ndc (package): 83262-002-01
ndc (product): 83262-002
ndc11 (package): 83262000201
spl id: 4615f01d-246f-7fbd-e063-6394a90a7a21
spl set id: f7fb6ac9-a920-a440-e053-6394a90aaa35

Reported adverse events (FAERS/openFDA)#

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