TIDL PAIN RELIEF HEAT THERAPY SPRAY.- pain relief heat therapy spray spray

TIDL PAIN RELIEF HEAT THERAPY Spray. by

Drug Labeling and Warnings

TIDL PAIN RELIEF HEAT 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

Camphor 10.5%
Lidocaine 4%

Purpose

Topical Anesthetic

Use

Temporary relief from minor aches and pains.

Warnings

For external use only.Contains coconut extract.

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. If pregnant or breast-feeding，ask a healthcare professional before 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, Angelica Sinensis Extract, Beta-Caryophyllene（Clove), Chili Extract, Coconut Extract, Dimethyl Sulfoxide, Green Tea Extract，Isopropyl Myristate, Peach Kernel Extract, Ligusticum Wallichii Extract, Propylene Glycol, Red Peony Flower Extract, Safflower Extract, Water, Oil of Wintergreen.

Questions

Call 1(888) 778-2986

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TIDL PAIN RELIEF HEAT THERAPY SPRAY. 
pain relief heat therapy spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84214-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	10.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
CARYOPHYLLENE (UNII: BHW853AU9H)
COCONUT (UNII: 3RT3536DHY)
CAPSAICIN (UNII: S07O44R1ZM)
LIGUSTICUM WALLICHII WHOLE (UNII: 8Y1N3NX2DW)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PAEONIA LACTIFLORA WHOLE (UNII: N44H57P7WG)
METHYL SALICYLATE (UNII: LAV5U5022Y)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
WATER (UNII: 059QF0KO0R)
SAFFLOWER (UNII: 4VBL71TY4Y)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
PRUNUS PERSICA SEED (UNII: V9C81470RR)
ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84214-004-01	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(84214-004)