MAMISAN PAIN RELIEVING CREAM LIDOCAINE PLUS MENTHOL- lidocaine hydrochloride, menthol cream 
PLANTIMEX DISTRIBUTORS INC

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Mamisan Pain Relieving Cream Lidocaine Plus Menthol

Drug Facts

Active Ingredients

Lidocaine HCl 4%

Menthol 1%

Purpose

Topical anesthetic

Topical analgesic

Use

temporarily relieves minor pain

Warnings

For external use only

Do not use

  • on large areas of the body or on cut, irritated or swollen skin
  • on puncture wounds
  • for more than one week without consulting a doctor

When using this product

  • use only as directed. Read and follow all directions and warnings on this label
  • rare cases of serious burns have been reported with products of this type
  • do not bandage tightly or apply local heat (such as heating pads) to the area of use with a medicated patch
  • avoid contact with the eyes and mucous membranes.
  • a transient burning sensation may occur upon application but generally disappears in several days.

Stop use and ask doctor if

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

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 right away.

Directions

apply a thin layer to affected area 6 to 8 hours, not to exceed 3 applications in a 24 hour period.

Inactive Ingredients

purified water, eucalyptus, PNC 400 and phenochem.

Package Labeling:

Outer PackageInner Package

MAMISAN PAIN RELIEVING CREAM LIDOCAINE PLUS MENTHOL 
lidocaine hydrochloride, menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72816-001
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
WATER (UNII: 059QF0KO0R)  
EUCALYPTUS GUM (UNII: 72T9EZC2VX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72816-001-0176.6 g in 1 BOTTLE; Type 0: Not a Combination Product06/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/19/2023
Labeler - PLANTIMEX DISTRIBUTORS INC (185464463)

Revised: 12/2023
Document Id: 0d6d2af4-b01b-4364-e063-6394a90aa990
Set id: 28078f3e-5bc4-4a98-b3cb-32c0af428469
Version: 2
Effective Time: 20231226
 
PLANTIMEX DISTRIBUTORS INC