TEETER RENEW MUSCLES PAIN RELIEVING- methyl salicylate, menthol cream

Teeter Renew Muscles Pain Relieving by

Drug Labeling and Warnings

Teeter Renew Muscles Pain Relieving by is a Otc medication manufactured, distributed, or labeled by STL International INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Methyl Salicylate 10.0%

Menthol 7.0%

Purpose

Topical Analgesic

Uses

Temporary relief of minor aches and pains of muscles and joints associated with:

simple backache arthritis strains bruises sprains

Warnings

For external use only.

Allergy Alert:

If you had prior allergic reaction to aspirin or salicylate, please consult a doctor before use.

Do not use

on wounds or damaged skin with a heating pad

Ask a physician before use if you have

redness over the affected area.

When using this product

avoid contact with eyes and mucus membranes do not bandage tightly

Stop use and ask a physician if

condition worsens or symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

excessive skin irritation occurs

pregnant or breastfeeding

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

Use only as directed

Adults and children 2 years of age or older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: consult a physician

Other information

Store at 20° to 25°C (68°-77°F)

Inactive Ingredients

Aqua (deionized water), arnica montana (arnica) extract, boswellia serrata extract, C13-14 isoparaffin, cetyl alcohol, citrus aurantium dulcis (orange) peel oil, chondroitin sulfate, dimethyl sulfone (MSM), emu oil, ethoxydiglycol, gluconolactone, glucosamine sulfate, glycerin, glyceryl stearate, isopropyl myristate, laureth-7, PEG-100 stearate, polyacrylamide, polysorbate-20, sodium benzoate, stearic acid.

Package Labeling

INGREDIENTS AND APPEARANCE

TEETER RENEW MUSCLES PAIN RELIEVING 
methyl salicylate, menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70329-730
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	100 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	70 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
CETYL ALCOHOL (UNII: 936JST6JCN)
ORANGE OIL (UNII: AKN3KSD11B)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EMU OIL (UNII: 344821WD61)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
LAURETH-7 (UNII: Z95S6G8201)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70329-730-01	1 in 1 BOX	02/09/2017
1		5 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	03/12/2016

Labeler - STL International INC (062729769)