OTC - ACTIVE INGREDIENT SECTION
Active ingredients Purpose
dl-Camphor 3% ....................................... Topical analgesic
dL-Menthol 15% ......................................... Topical analgesic
Active ingredients Purpose
dl-Camphor 3% ....................................... Topical analgesic
dL-Menthol 15% ......................................... Topical analgesic
Uses
Temporarily relieves aches and pains of muscles and joints associated with one or more of the following:simple backache, lumbago, strains and sprains (involving muscles, tendons and /or ligaments) and arthritis.
Not recommended for emotional pain. Consult a healthcare practitioner / health care provider / health care professional / doctor / physician for use beyond 7 days.
Warnings
For external use only
• Avoid contact with the eyes and mucous membranes. Do ont use otherwise than as directed.
Caution: Discontinue use if excessive irritation of the skin develops.
When using this product
Do not apply to wounds or damaged skin.
Do not tightly bandage.
Do not apply with external heat, such as electric heating pad, as this may result in excessive skin irritation or skin burn.
Do not inhale.
Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if • Hypersensitivity / allergy, rashes and or burning discomfort occur. • You experience pain, swelling or blistering. •Symptoms worsens •Symptoms persist for more than 7 days or clear up and occur again within a few days.
If pregnant or breast-feeding, ask a health professional before use.
Seek immediate medical help or contact a Poison Control Center immediately if overdose or accidental ingestion occurs.
Directions
Adults and children 12 years of age and older: 1 Spray 3-4 times per day. Apply thinly and evenly to affected area. Rub and / or massage into skin until solution vannishes.
Children under 12 years of age: Consult a doctor.
beta-Alanine, Magnesium chloride, SDAG-3, Salix Nigra (Willow) Bark Extract, Aqua (Water), Glycerin, Potassium chloride.
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73646-001-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-225d-111a-e063-dadaa90a10e2 | Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73646-001-01 | TRIUMPH DAILY MD | 120 mL in 1 BOTTLE, SPRAY | SPRAY | 120 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 73646-001 | 73646-001-01 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | ACTIB |
| RACEMENTHOL | YS08XHA860 | ACTIB |
| WILLOW BARK | S883J9JDYX | IACT |
| SALIX ALBA BARK | 205MXS71H7 | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| .BETA.-ALANINE | 11P2JDE17B | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| MAGNESIUM CHLORIDE | 02F3473H9O | IACT |
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 |
|---|---|---|---|---|---|---|
| c8ba7005-a8ee-417c-8015-be2a416cdc42 | da2e00c8-b60b-4ff2-a5d1-5467d6ee2db4 | 2020-02-17 | Warnings | c8ba7005-a8ee-417c-8015-be2a416cdc42 da2e00c8-b60b-4ff2-a5d1-5467d6ee2db4 |
Adverse event summaries are temporarily unavailable. Other product information remains available.