Teevodar Pain Relieving

Manufacturer: Sod-e Biotech Ltd
Effective date: 2025-12-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:26:04

Label at a glance#

ProductTeevodar Pain Relieving

Active ingredientMENTHOL

Label structure8 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

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: Do not use, consult a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

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.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes
do not apply to wounds or damaged skin
do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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: Do not use, consult a doctor.

Other information

OTHER SAFETY INFORMATION

You may report serious side effects to: Dorrington LLC, 7 Skyline Dr., Suite 350, Hawthorne, NY 10532

Inactive ingredients

INACTIVE INGREDIENT SECTION

butyrospermum parkii (shea) butter, ceteareth-20, cetearyl alcohol, cetyl alcohol, citric acid, dimethicone, ethylhexlglycerin, isopropyl myristate, lanolin, mentha spicata leaf, origanum vulgare leaf extract, paraffinum liquidum, petrolatum, phenoxyethanol, purified water, rosmarinus officinalis leaf extract, zea mays oil

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
416982	menthol 1.25 % Topical Cream	PSN	2
416982	menthol 12.5 MG/ML Topical Cream	SCD	2
416982	menthol 1.25 % Topical Cream	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906	Product name	7	20210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
84483-0001-1	Teevodar Pain Relieving	1 in 1 BOX	CREAM	1	2
84483-0001-1	Teevodar Pain Relieving	50 g in 1 TUBE	CREAM	50	2
84483-0001-2	Teevodar Pain Relieving	5 g in 1 PACKET	CREAM	5	2

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

Teevodar Pain Relieving
Menthol
CETOSTEARYL ALCOHOL
PHENOXYETHANOL
SPEARMINT
ISOPROPYL MYRISTATE
CETYL ALCOHOL
ANHYDROUS CITRIC ACID
OREGANO
PETROLATUM
SHEA BUTTER
POLYOXYL 20 CETOSTEARYL ETHER
LANOLIN
MINERAL OIL
WATER
ROSEMARY
DIMETHICONE
ETHYLHEXYLGLYCERIN
CORN OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84483-0001	84483-0001-1, 84483-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CETOSTEARYL ALCOHOL	2DMT128M1S	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
SPEARMINT	J7I2T6IV1N	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
CETYL ALCOHOL	936JST6JCN	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
OREGANO	0E5AT8T16U	IACT
PETROLATUM	4T6H12BN9U	IACT
SHEA BUTTER	K49155WL9Y	IACT
POLYOXYL 20 CETOSTEARYL ETHER	YRC528SWUY	IACT
LANOLIN	7EV65EAW6H	IACT
MINERAL OIL	T5L8T28FGP	IACT
WATER	059QF0KO0R	IACT
ROSEMARY	IJ67X351P9	IACT
DIMETHICONE	92RU3N3Y1O	IACT
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
CORN OIL	8470G57WFM	IACT
MENTHOL	L7T10EIP3A	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
Teevodar Pain Relieving	MENTHOL	Sod-e Biotech Ltd	205b0fef-4f00-db2e-e063-6294a90a93b8	2025-12-17	Warnings	Exact identifier ndc (package): 84483-0001-2 ndc (package): 84483-0001-1 ndc (product): 84483-0001 ndc11 (package): 84483000102 ndc11 (package): 84483000101 spl id: 462d75d3-2990-628b-e063-6294a90a99c8 spl set id: 205b0fef-4f00-db2e-e063-6294a90a93b8

Reported adverse events (FAERS/openFDA)#

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