CM Cream

Manufacturer
Youngevity International Inc. | Creative Essences Inc
Effective date
2025-10-22
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:40:31

Label at a glance#

ProductTopical Analgesic
Active ingredientMENTHOL
Label structure11 sections

Indications and uses

Temporary relief on minor aches and pains of sore muscles and joints associated with: Backaches arthritis strains bruises sprains

Dosage and administration

adults and children 2 years of age or older, apply to affected area no more than 3 to 4 times a day. children under 2 years of age, consult a doctor.

Storage and handling

Store in a cool, dry place

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.4%, Purpose: Topical Analgesic

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relief on minor aches and pains of sore muscles and joints associated with:

  • Backaches
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor

OTC - DO NOT USE SECTION

Stop use and ask a doctor if

  • condition worsens
  • symptoms persists for more than 7 day or clears up and occurs again within a few days

When using this product

OTC - WHEN USING SECTION

When using this product:

  • Keep out of eyes, ears, and mouth
  • In case of contact with eyes, rinse eyes thoroughly with water
  • Do not apply to wounds or damaged skin
  • Do not bandage tightly

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age or older, apply to affected area no more than 3 to 4 times a day.

children under 2 years of age, consult a doctor.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Carbomer, celadrin (cetyl myristoleate, cetyl myristate, cetyl palmitaoleate, cetyl oleate, cetyl laurate), cetyl alcohol, ethylhexylglycerin, glycerin, glyceryl monostearate, myristyl alcohol, olive oil, peppermint oil, phenoxyethanol, polysorbate 20, propylene glycol, stearic acid, triethanolamine, water

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CM Cream LabelCM Cream LabelUltimate CM Cream Muscle and Joint Support 2 fl oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2391332menthol 1.4 % Topical CreamPSN7
2391332menthol 14 MG/ML Topical CreamSCD7
2391332menthol 1.4 % Topical CreamSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80986-101-01Topical Analgesic59 g in 1 JARCREAM597

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80986-10180986-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62025-03-26full-release2026-06-01 00:57:51

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
Topical AnalgesicMENTHOLYoungevity International Inc.b4693947-f5b3-6fd3-e053-2995a90ab5812025-10-22WarningsExact identifier
ndc (package): 80986-101-01
ndc (product): 80986-101
ndc11 (package): 80986010101
spl id: 41ca9fa1-0b43-425a-e063-6394a90afac0
spl set id: b4693947-f5b3-6fd3-e053-2995a90ab581

Reported adverse events (FAERS/openFDA)#

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