Indications and uses
For the temporary relief of minor aches and pains of muscles and joints associated with: simple backache arthritis strains bruises sprains
Relieve Your Pain
- Manufacturer
- SOLITEINT Kozmetikum gyarto es forgalmazo, termelo es kereskedelmi Korlatolt Felelossegu Tarsasag | SOLITEINT Ko zmetikum gyarto es fo rgalmazo termelo es kereskedelmi Ko rlato lt Felelo ssegu Tarsasag
- Effective date
- 2022-02-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:48:14
Label at a glance#
ProductRelieve Your Pain
Active ingredientMENTHOL
Label structure9 sections
Dosage and administration
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
Storage and handling
Store in a cool, dry place. Avoid direct sunlight. Tamper-evident for your protection. Use only if safety seal is intact. Keep away from excessive heat or flame.
Contacts and useful links#
Label contents#
Full prescribing information#
Active Ingredients
Menthol USP 10%
Purpose
Menthol USP 10%.....................Topical Analgesic
Uses
For the temporary relief of minor aches and pains of muscles and joints associated with:
- simple backache
- arthritis
- strains
- bruises
- sprains
Warnings
Use only as directed. For external use only.
OTC - WHEN USING SECTION
When using this product:
- avoid contact with eyes and mucous membranes
- do not apply to wounds or damaged skin
- do not bandage or use with a heating pad, other ointments, creams, sprays, or liniments.
OTC - STOP USE SECTION
Stop use and ask doctor if:
- condition worsens
- symptoms persist for more than 7 days, or clear up and reoccur again within a few days
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.
Directions
Adults and children 2 years of age and older:
- Apply to affected area not more than 3 to 4 times daily.
Other Information
- Store in a cool, dry place.
- Avoid direct sunlight.
- Tamper-evident for your protection. Use only if safety seal is intact.
- Keep away from excessive heat or flame.
Inactive Ingredients
Aqua, Magnesium Chloride, Dimethyl Sulfone (Methylsulfonylmethane), Glyceryl Stearate SE, Cetearyl Alcohol, Sweet Almond Oil (Prunus Amygdalus Dulcis), Shea Butter (Butyrospermum Parkii), Ceteareth-20, Glycerin, Pentylene Glycol, Undecane, Tocopheryl Acetate, Cetyl Palmitate, Arnica Montana Flower Extract, Tocopherol, Xanthan Gum, Tridecane, Sodium Chloride, Potassium Chloride, Magnesium Sulfate, Calcium Chloride, Ascorbyl Palmitate, Hydroxyacetophenone
Questions or Comments?
888-819-6472; Monday-Friday, 9am-5pm CT
Report any serious side effects to number above.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 72683-005-01
Non-toxic
Paraben Free
Asutra*
Relieve
your
pain
10% Menthol
Pain Relief Cream
With Moisturizing
Magnesium and
Arnica Montana
Net Wt. 3.4 oz. | 96 g.
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75249-005-01 | 2024-07-30 | C162847 | 48780-1 | 1e7a6dab-1d2d-a2ce-e063-dadaa90aadf7 | Asutra Relieve Your Pain |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75249-005-01 | Relieve Your Pain | 96 g in 1 TUBE | CREAM | 96 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 75249-005 | RELIEVE YOUR PAIN (MENTHOL) CREAM [SOLITEINT KOZMETIKUM GYARTO ES FORGALMAZO, TERMELO ES KERESKEDELMI KORLATOLT FELELOSSEGU TARSASAG] | 1 | Legacy NDC, 1 package rows | 20220212_d7c78f30-1c21-1dbb-e053-2995a90a4f64.zip |
Products#
Every source-derived product name is available through these pages.
- Relieve Your Pain
- Menthol
- TRIDECANE
- GLYCERIN
- PENTYLENE GLYCOL
- ALPHA-TOCOPHEROL ACETATE
- CETYL PALMITATE
- ARNICA MONTANA FLOWER
- TOCOPHEROL
- XANTHAN GUM
- POTASSIUM CHLORIDE
- MAGNESIUM SULFATE, UNSPECIFIED FORM
- CALCIUM CHLORIDE
- HYDROXYACETOPHENONE
- SODIUM CHLORIDE
- SHEA BUTTER
- POLYOXYL 20 CETOSTEARYL ETHER
- UNDECANE
- ASCORBYL PALMITATE
- DIMETHYL SULFONE
- WATER
- MAGNESIUM CHLORIDE
- GLYCERYL STEARATE SE
- ALMOND OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75249-005 | 75249-005-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| d7c78f30-1c22-1dbb-e053-2995a90a4f64 | d7c78f30-1c21-1dbb-e053-2995a90a4f64 | 2022-02-11 | Warnings | d7c78f30-1c22-1dbb-e053-2995a90a4f64 d7c78f30-1c21-1dbb-e053-2995a90a4f64 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.