MMM Ice Gel

Manufacturer
Southern Sales & Services, Inc
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:28

Label at a glance#

ProductMMM Ice Gel
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure12 sections

Storage and handling

Other information • do not freeze • Keep lid tightly closed

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Menthol 2.0% Purpose: Topical Analgesic

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with

  • Simple backache
  • Arthritis
  • Strains
  • Bruises
  • Sprains

WARNINGS SECTION

For external use only. Avoid contact with eyes.

OTC - WHEN USING SECTION

• do not bandage tightly
• do not apply to wounds or damaged skin

OTC - STOP USE SECTION

Stop use and ask a doctor if

• condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

STORAGE AND HANDLING SECTION

Other information

• do not freeze
• Keep lid tightly closed

INACTIVE INGREDIENT SECTION

Inactive ingredients carbomer, propylene glycol, methylparaben, isopropyl alcohol, triethanol- amine, FD&C Blue no. 1, purified water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

227 g NDC: 69822-013-80

MMM Therapeutic Ice Gel

Topical Analgesic

Net Wt. 8 oz

MMM Ice GelMMM Ice Gel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311502menthol 2 % Topical GelPSN1
311502menthol 0.02 MG/MG Topical GelSCD1
311502menthol 2 % Topical GelSY1
311502menthol 2 % topical stickSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69822-013-802023-01-30C16284748780-1f386c64a-3119-0266-e053-dadaa90a7c1aMMM Therapeutic Ice Gel Topical Analgesic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69822-013-80MMM Ice Gel227 g in 1 BOTTLE, PLASTICGEL2271

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69822-013MMM ICE GEL (MENTHOL) GEL [SOUTHERN SALES & SERVICES, INC]1Legacy NDC, 1 package rows20210923_c5ec7276-8b63-4bdb-e053-2995a90a2217.zip

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
69822-01369822-013-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
c5ec7276-8b64-4bdb-e053-2995a90a2217c5ec7276-8b63-4bdb-e053-2995a90a22172021-01-01WarningsExact identifier
spl id: c5ec7276-8b64-4bdb-e053-2995a90a2217
spl set id: c5ec7276-8b63-4bdb-e053-2995a90a2217

Reported adverse events (FAERS/openFDA)#

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