Dosage and administration
- Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. - Children under two years of age: consult a physician.
DAREDEVIL STRENGTH Muscle and Arthritis Pain Relieving Roll On
- Manufacturer
- DDR Products, LLC
- Effective date
- 2018-11-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:45:07
Label at a glance#
ProductDAREDEVIL STRENGTH Muscle and Arthritis Pain Relieving Roll On
Active ingredientMENTHOL
Label structure7 sections
Label contents#
Full prescribing information#
Active Ingredient:
Menthol 10.00%
OTC - PURPOSE SECTION
Topical Analgesic
Indications:
For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.
Warnings:
- For external use only.
- Avoid contact with eyes.
- If symptoms persist for more than seven days, discontinue use and consult physician.
Keep out of reach od children.
If swallowed, consult physician.
Do not apply
- to wounds or damaged skin.
- Do not bandage tightly.
- If pregnant or breast feeding,
contact physician prior to use.
Directions:
- Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
- Children under two years of age: consult a physician.
Additional Information:
Store at room temperature.
Other Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Carbomer, Glycerin, Magnesium Sulfate, Phenoxyethanol, SD-Alcohol 40B, Sodium Hydroxide, Tocopheryl Acetate (Vitamin E), Xanthan Gum.
Package Labeling:
Products#
Every source-derived product name is available through these pages.
- DAREDEVIL STRENGTH Muscle and Arthritis Pain Relieving Roll On
- MENTHOL
- ALOE VERA LEAF
- WATER
- CARBOXYPOLYMETHYLENE
- GLYCERIN
- MAGNESIUM SULFATE, UNSPECIFIED FORM
- PHENOXYETHANOL
- SODIUM HYDROXIDE
- XANTHAN GUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71977-010 | 71977-010-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| CARBOXYPOLYMETHYLENE | 0A5MM307FC | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| MAGNESIUM SULFATE, UNSPECIFIED FORM | DE08037SAB | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 07214fe7-2a23-b832-e063-6294a90a3df7 | 2764574f-381f-41e6-85d7-d8f3ce474075 | 2023-10-07 | Warnings | 2764574f-381f-41e6-85d7-d8f3ce474075 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.