NAMMAN MUAY PAIN RELIEVING- menthol, methyl salicylate liniment

Namman Muay Pain Relieving by

Drug Labeling and Warnings

Namman Muay Pain Relieving by is a Otc medication manufactured, distributed, or labeled by Devakam Apothecary Hall, Co, Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Menthol 1.25%

Methyl Salicylate 31%

Purpose

Counterirritant

Uses

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

• simple backache
• arthritis
• strains
• bruises
• sprains

Warnings

For external use only. Avoid contact with the eyes and mucous membranes.

Ask a doctor before use if you have 

allergic reactions to aspirin or salicylates.

When using this product

• use only as directed 
• do not apply to wounds or damaged skin
• do not bandage tightly or use with a heating pad

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
• redness is present
• irritation of the skin develops

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away

​Directions

• Massage into affected area until thoroughly absorbed into the skin.
• Shake well before use.
• Fod individuals 12 years of age and older:  Apply generously to the affected area not more than 4 times daily.
• Children under 12 years of age: Consult a doctor.

Inactive ingredients

Alcohol, DC Red#17, DC Yellow#11, Disodium EDTA, Eucalyptus Oil, Mineral Oil, Polysorbate 80, Purified Water

Package Labeling:

INGREDIENTS AND APPEARANCE

NAMMAN MUAY PAIN RELIEVING 
menthol, methyl salicylate liniment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43599-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	12.5 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	310 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
D&C RED NO. 17 (UNII: ND733RX3JN)
D&C YELLOW NO. 11 (UNII: 44F3HYL954)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
EUCALYPTUS OIL (UNII: 2R04ONI662)
MINERAL OIL (UNII: T5L8T28FGP)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43599-000-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	08/01/2020

Labeler - Devakam Apothecary Hall, Co, Ltd. (661733091)