Dosage and administration
Directions: Adult and children 2 years of age and older: apply to affected area up to 4 times daily. Rub in gently. Children under 2 years of age: consult a doctor. Patch test recommended on sensitive skin.
Triflora
- Manufacturer
- Schwabe North America, Inc | Schwabe Mexico SA DE CV
- Effective date
- 2021-10-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 11
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:34:24
Label at a glance#
ProductTriflora
Active ingredientURTICA DIOICA, TOXICODENDRON PUBESCENS LEAF, LEDUM PALUSTRE twig
Label structure11 sections
Label contents#
Full prescribing information#
Active Ingredients
URTICA DIOICA 1X
LEDUM PALUSTRE 2X
RHUS TOX 3X
Inactive Ingredient
PURIFIED WATER
ETHYL ALCOHOL
WITCH HAZEL DISTILLATE
POLYARLYLIC ACID
PINE NEEDLE OIL
SODIUM HYDROXIDE
Dosage and Administration
Directions:
Adult and children 2 years of age and older: apply to affected area up to 4 times daily.
Rub in gently.
Children under 2 years of age: consult a doctor.
Patch test recommended on sensitive skin.
Indications & Usage
Temporarily relieves minor aches, pains, and joint/muscle stiffness associated with arthritis, rheumatism, simple backache and tendinitis.
Purpose
Temporarily relieves minor aches, pains, and joint/muscle stiffness associated with arthritis, rheumatism, simple backache and tendinitis.
Warning
For external use only.
Avoid contact with eyes and broken skin.
Do Not Use
Do not use if hypersensitive to this or any other ingredients in this product; this product contains poison ivy (Rhus tox) plant materials.
Stop Use
Stop use and ask a doctor if skin irritation, rash or other allergic reaction develops, condition worsens or does not improve within 7 days, symptoms clear up and occur again within a few days.
These could be sigs of a serious condition.
Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a healthcare professional before use.
Keep out of reach of children
Keep out of reach of children.
Overdose
If swallowed, seek medical help or contact a Poison Control Center immediately.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Triflora
- Urtica doicia, Rhus Toxicodendron, Ledum Palustre
- URTICA DIOICA
- TOXICODENDRON PUBESCENS LEAF
- LEDUM PALUSTRE twig
- CARBOMER HOMOPOLYMER TYPE C
- ALCOHOL
- PINE NEEDLE OIL (PINUS SYLVESTRIS)
- WATER
- SODIUM HYDROXIDE
- WITCH HAZEL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53499-6290 | 53499-6290-8, 53499-6290-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| URTICA DIOICA | 710FLW4U46 | ACTIB |
| TOXICODENDRON PUBESCENS LEAF | 6IO182RP7A | ACTIB |
| LEDUM PALUSTRE twig | 877L01IZ0P | ACTIB |
| CARBOMER HOMOPOLYMER TYPE C | 4Q93RCW27E | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| PINE NEEDLE OIL (PINUS SYLVESTRIS) | 5EXL5H740Y | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| WITCH HAZEL | 101I4J0U34 | IACT |
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 |
|---|---|---|---|---|---|---|
| 7fd55ef8-9a5f-48eb-bc41-152d5e2a3aa9 | 7dd55ac1-e1d2-4404-9e33-2578aee719e3 | 2021-10-01 | Warnings | 7fd55ef8-9a5f-48eb-bc41-152d5e2a3aa9 7dd55ac1-e1d2-4404-9e33-2578aee719e3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.