MMM ICE GEL- menthol gel 
Southern Sales & Services, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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MMM Therapeutic Ice Gel
Topical Analgesic

Active Ingredients Menthol 2.0% Purpose: Topical Analgesic

Topical Analgesic

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

For external use only. Avoid contact with eyes.

• 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 within a few days.

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

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

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.

Other information

• do not freeze
• Keep lid tightly closed

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

227 g NDC: 69822-013-80

MMM Therapeutic Ice Gel

Topical Analgesic

Net Wt. 8 oz

MMM Ice Gel

MMM ICE GEL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69822-013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69822-013-80227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/01/2021
Labeler - Southern Sales & Services, Inc (013114906)
Registrant - Southern Sales & Services, Inc (013114906)
Establishment
NameAddressID/FEIBusiness Operations
Southern Sales & Services, Inc013114906label(69822-013)

Revised: 1/2021
Document Id: c5ec7276-8b64-4bdb-e053-2995a90a2217
Set id: c5ec7276-8b63-4bdb-e053-2995a90a2217
Version: 1
Effective Time: 20210101
 
Southern Sales & Services, Inc