Mamisan Pain Relieving Ointment

Mamisan Pain Relieving by

Drug Labeling and Warnings

Mamisan Pain Relieving by is a Otc medication manufactured, distributed, or labeled by PLANTIMEX DISTRIBUTORS INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAMISAN PAIN RELIEVING- lidocaine hydrochloride, menthol ointment 
PLANTIMEX DISTRIBUTORS INC

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Mamisan Pain Relieving Ointment

Drug Facts

Active ingredients

Lidocaine HCl 4%

Menthol 1%

Purpose

Pain relieving

Use

  • For the temporary relief of pain

Warnings

For external use only.

When using this product

  • avoid contact with the eyes

do not use

  • in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if

condition worsens, or if 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 right away.

Directions

  • 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

Store in a cool, dry place 68-77°F (20-25°C)

Inactive ingredients

BHT, D&C Red #17, D&C Yellow #11, Eucalyptus Oil, Petrolatum, Soybean Oil, Wax.

Package Labeling:

Label

Package Labeling:72816-000-02

Label02

MAMISAN PAIN RELIEVING 
lidocaine hydrochloride, menthol ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72816-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
D&C RED NO. 17 (UNII: ND733RX3JN)  
D&C YELLOW NO. 11 (UNII: 44F3HYL954)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
PETROLATUM (UNII: 4T6H12BN9U)  
SOYBEAN OIL (UNII: 241ATL177A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72816-000-01200 g in 1 BOTTLE; Type 0: Not a Combination Product06/05/202306/12/2024
2NDC: 72816-000-02100 g in 1 JAR; Type 0: Not a Combination Product06/12/202306/12/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/05/202306/12/2024
Labeler - PLANTIMEX DISTRIBUTORS INC (185464463)

Revised: 6/2024
Document Id: 1b4045cb-4123-6b27-e063-6294a90aa757
Set id: b3c2759d-d064-3522-e053-2a95a90add73
Version: 6
Effective Time: 20240619