Namman Muay Pain Relieving

Manufacturer: Devakam Apothecary Hall, Co, Ltd.
Effective date: 2020-10-02
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:30:53

Label at a glance#

ProductNamman Muay Pain Relieving

Active ingredientMENTHOL, METHYL SALICYLATE

Label structure6 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains

Dosage and administration

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Methyl Salicylate 31%

Purpose

OTC - PURPOSE SECTION

Counterirritant

Uses

INDICATIONS & USAGE SECTION

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

simple backache
arthritis
strains
bruises
sprains

Warnings

WARNINGS SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

allergic reactions to aspirin or salicylates.

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1426141	menthol 1.25 % / methyl salicylate 31 % Topical Solution	PSN	2
1426141	menthol 12.5 MG/ML / methyl salicylate 310 MG/ML Topical Solution	SCD	2
1426141	menthol 1.25 % / methyl salicylate 31 % Topical Liniment	SY	2
1426141	menthol 1.25 % / methyl salicylate 31 % Topical Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43599-000-04	2023-01-30	C162847	48780-1	f386c649-9d67-0266-e053-dadaa90a7c1a	Namman Muay Pain Relieving Liniment

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43599-000-04	Namman Muay Pain Relieving	120 mL in 1 BOTTLE	LINIMENT	120		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43599-000	NAMMAN MUAY PAIN RELIEVING (MENTHOL, METHYL SALICYLATE) LINIMENT [DEVAKAM APOTHECARY HALL, CO, LTD.]	2	Legacy NDC, 1 package rows	20201003_a834bf80-5b9a-aee4-e053-2a95a90a82a0.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Namman Muay Pain Relieving
MENTHOL, METHYL SALICYLATE
ALCOHOL
D&C RED NO. 17
D&C YELLOW NO. 11
EDETATE DISODIUM ANHYDROUS
EUCALYPTUS OIL
MINERAL OIL
POLYSORBATE 80
WATER
MENTHOL
METHYL SALICYLATE
SALICYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43599-000	43599-000-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
D&C RED NO. 17	ND733RX3JN	IACT
D&C YELLOW NO. 11	44F3HYL954	IACT
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
MINERAL OIL	T5L8T28FGP	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
WATER	059QF0KO0R	IACT
MENTHOL	L7T10EIP3A	ACTIB
METHYL SALICYLATE	LAV5U5022Y	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b0b54003-2835-c30b-e053-2a95a90af88f			a834bf80-5b9a-aee4-e053-2a95a90a82a0	2020-10-02	Warnings	Exact identifier spl id: b0b54003-2835-c30b-e053-2a95a90af88f spl set id: a834bf80-5b9a-aee4-e053-2a95a90a82a0

Reported adverse events (FAERS/openFDA)#

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