FDA.reportPublic FDA data

MMM Topical Analgesic Cream

Manufacturer
Southern Sales & Services, Inc.
Effective date
2021-09-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:29

Label at a glance#

ProductMMM Topical Analgesic Cream
Active ingredientMETHYL SALICYLATE, MENTHOL
Label structure11 sections

Storage and handling

Store: At Room Temperature 15° - 30°C (59°- 86°F). Close cap tightly after use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 8%

Menthol 2%

OTC - PURPOSE SECTION

Topical Analgesic

OTC - DO NOT USE SECTION

Stop use and ask a doctor if

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

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

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

WARNINGS SECTION

For external use only.

  • avoid contact with eyes and mucous membranes
  • do not use otherwise than as directed

Caution: Discontinue use if excessive irritation of the skin develops.

When using this product

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

Stop use and ask a doctor if

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

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

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

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints due to:

  • arthritis
  • simple backache
  • strains
  • sprains
  • bruises

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

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

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 Immediately.

DOSAGE & ADMINISTRATION SECTION

Adults and Children 12 Years of Age or Older: Apply to affected area not more than 3 to 4 times daily.

Children under 12 year of age: consult a doctor

STORAGE AND HANDLING SECTION

Store: At Room Temperature 15° - 30°C (59°- 86°F).

Close cap tightly after use.

INACTIVE INGREDIENT SECTION

mineral oil, propylene glycol, cetyl stearyl alcohol, purified water, ceteareth-6, stearyl alcohol, PEG-20 cetyl/stearyl ether, methylparaben, propylparaben.

MMM Topical Analgesic Cream

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MMM Analgesic CreamMMM Analgesic Cream

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1438766methyl salicylate 8 % / menthol 2 % Topical CreamPSN1
1438766menthol 20 MG/ML / methyl salicylate 80 MG/ML Topical CreamSCD1
1438766methyl salicylate 8 % / menthol 2 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69822-030-202023-01-30C16284748780-1f386c649-9d49-0266-e053-dadaa90a7c1aMMM Topical Analgesic Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69822-030-20MMM Topical Analgesic Cream60 g in 1 TUBECREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69822-030MMM TOPICAL ANALGESIC CREAM (METHYL SALICYLATE AND MENTHOL CREAM) CREAM [SOUTHERN SALES & SERVICES, INC.]1Legacy NDC, 1 package rows20210923_cc877b45-277c-c279-e053-2995a90a8b36.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69822-03069822-030-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARYL ALCOHOL2KR89I4H1YIACT
MINERAL OILT5L8T28FGPIACT
METHYL SALICYLATELAV5U5022YACTIB
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CETEARETH-62RJS3559D3IACT

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
cc877b45-277d-c279-e053-2995a90a8b36cc877b45-277c-c279-e053-2995a90a8b362021-09-21WarningsExact identifier
spl id: cc877b45-277d-c279-e053-2995a90a8b36
spl set id: cc877b45-277c-c279-e053-2995a90a8b36

Reported adverse events (FAERS/openFDA)#

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