TIDL PAIN RELIEF EVENING THERAPY SPRAY.- pain relief evening therapy spray spray

Tidl Pain Relief Evening Therapy Spray. by

Drug Labeling and Warnings

Tidl Pain Relief Evening Therapy Spray. by is a Otc medication manufactured, distributed, or labeled by Shenzhen Sam Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 1%
Lidocaine 4%

Purpose

Topical Anesthetic

Use

Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains

Warnings

For external use only

Do not use

While smoking or near heat or open flame

When Using

·avoid contact with the eyes or mucous membranes
·do not apply to wounds or damaged skin
·do not apply to irritated skin
·do not bandage
·wash hands after use with cool water
·do not use with heating pad or device
·spray product away from nose,eyes,and mouth

Stop Use

if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Ask Doctor

if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days

Keep Oot Of Reach Of Children

If accidentally ingested get medical help or contact a Poison Control Center immediately. Make sure to turn child safety spray lock to off position when not in use.

Directions

·Adults and children 12 years of age and older：Apply to affected area not more than 3 to 4 times daily
·Children under 12 years of age：Consult physician

Inactive ingredients

Alcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene（Clove）, Calendula Officinalis Flower, Chamomile Extract, Chorus Fruit Extract，Dimethyl Sulfoxide, Echinacea Angustifolia Extract, Green Tea Extract，Hyaluronic Acid，IIex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Lavender Extract, Water, White Willow Bark Extract, Oil of Wintergreen.

Questions

Call 1(888) 778-2986

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TIDL PAIN RELIEF EVENING THERAPY SPRAY. 
pain relief evening therapy spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84214-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
HYALURONIC ACID (UNII: S270N0TRQY)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CITRUS FRUIT (UNII: XDK00Z8012)
JUNIPER BERRY (UNII: O84B5194RL)
METHYL SALICYLATE (UNII: LAV5U5022Y)
CARYOPHYLLENE (UNII: BHW853AU9H)
CHAMOMILE (UNII: FGL3685T2X)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
SALIX ALBA BARK (UNII: 205MXS71H7)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84214-007-01	90 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/13/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/13/2024

Labeler - Shenzhen Sam Technology Co., Ltd. (418511877)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Sam Technology Co., Ltd.		418511877	manufacture(84214-007)