Dosage and administration
·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
·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
Menthol 1%
Lidocaine 4%
Topical Anesthetic
Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains
For external use only
While smoking or near heat or open flame
·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
if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days
if condition worsens, or if symptoms persist for more than 7 days, or clear up and reoccur again within a few days
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.
·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
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.
Call 1(888) 778-2986
| Class | Version | Type | Effective |
|---|---|---|---|
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 070fbed5-7088-434a-a7ce-f2a64d8d40ac | Product name | 2 | 20260107 |
| bee66ce1-adb7-9d3b-67d9-582e4c54e80f | Product name | 5 | 20250819 |
| 860a93dc-4863-49cc-b284-6bbe8191bc48 | Product name | 4 | 20250214 |
| eaba870a-6a9d-442e-8643-87b3f558a451 | Product name | 1 | 20250117 |
| 9b4cf230-fd05-41d5-98c6-5db9ecb27b86 | Product name | 1 | 20230117 |
| 7d755fa1-1087-4dcd-98f0-6d4bba479a57 | Product name | 3 | 20210602 |
| aed701d5-9c75-dfaf-7154-cde46179faea | Product name | 9 | 20200313 |
| fa8b5901-e681-426f-82fe-54f6d81ec698 | Product name | 4 | 20180619 |
| 332d03e4-aa24-4b11-841a-02bf41081920 | Product name | 1 | 20171221 |
| c08ab52f-2fc8-4409-9d9f-ed8edc0bd070 | Product name | 1 | 20171221 |
| 68ed98f8-24c2-44a0-944a-6d36e82ce25a | Product name | 1 | 20141222 |
| 1cd42bc2-a430-c72b-636d-991b235fbf80 | Product name | 1 | 20140508 |
| 49fa150c-f0de-cce7-3d9c-993ed81c5698 | Product name | 1 | 20140508 |
| 4d7ae718-ed00-bae8-2abe-9eaec1eef7ff | Product name | 1 | 20140508 |
| 9137811f-f279-8640-5aeb-99fa2145d64d | Product name | 1 | 20140508 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84214-007-01 | Tidl Pain Relief Evening Therapy Spray. | 90 mL in 1 BOTTLE, SPRAY | SPRAY | 90 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 84214-007 | 84214-007-01 |
Every source-derived ingredient row is available through these pages.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Tidl Pain Relief Evening Therapy Spray. | PAIN RELIEF EVENING THERAPY SPRAY | Shenzhen Sam Technology Co., Ltd. | 1d1a2f4a-7b25-e595-e063-6394a90a00d5 | 2024-07-13 | Warnings | 84214-007-01 84214-007 84214000701 1d1a2f4a-7b26-e595-e063-6394a90a00d5 1d1a2f4a-7b25-e595-e063-6394a90a00d5 |
Adverse event summaries are temporarily unavailable. Other product information remains available.