TEEVODAR PAIN RELIEVING- menthol cream

Teevodar Pain Relieving by

Drug Labeling and Warnings

Teevodar Pain Relieving by is a Otc medication manufactured, distributed, or labeled by Sod-e Biotech Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Menthol 1.25%

Purpose

Topical analgesic

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.

When using this product

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

Stop use and ask a doctor if

• 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.

If swallowed, get medical help or contact a Poison Control Center 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: Do not use, consult a doctor.

Other information

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

Inactive ingredients

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

INGREDIENTS AND APPEARANCE

TEEVODAR PAIN RELIEVING 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84483-0001
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 g

Inactive Ingredients
Ingredient Name	Strength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SPEARMINT (UNII: J7I2T6IV1N)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CETYL ALCOHOL (UNII: 936JST6JCN)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
OREGANO (UNII: 0E5AT8T16U)
PETROLATUM (UNII: 4T6H12BN9U)
SHEA BUTTER (UNII: K49155WL9Y)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
LANOLIN (UNII: 7EV65EAW6H)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)
ROSEMARY (UNII: IJ67X351P9)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CORN OIL (UNII: 8470G57WFM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84483-0001-1	1 in 1 BOX	09/01/2024
1		50 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 84483-0001-2	5 g in 1 PACKET; Type 0: Not a Combination Product	09/01/2024	06/30/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/01/2024

Labeler - Sod-e Biotech Ltd (626018937)