Triflora description, usages, side effects, indications, overdosage, supplying and lots more!

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Triflora

Natures Way Holding Co.

Triflora




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients (HPUS): 

LEDUM PALUSTRE

RHUS TOXICODENDRON

SYMPHYTUM OFFICINALE


Inactive Ingredients:

CARBOMER HOMOPOLYMER TYPE C

ALCOHOL

PINE NEEDLE OIL (PINUS SYLVESTRIS)

WATER
SODIUM HYDROXIDE
WITCH HAZEL

Dosage and Administration:

Boericke and Tafel Brand:

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.

Uses

Indications and Usage:

Temporarily relieves minor aches, pains, and joint/muscle stiffness associated with arthritis, rheumatism, simple backache and tendinitis.

Purpose

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.  This product contains poison ivy (Rhus toxicodendron) plant materials.  Do not use if hypersensitive to this or any other ingredients in this product.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Children:

Keep out of the reach of children.

Pregnancy or Breast Feeding:

Breast-feeding women should not apply to breast area.

Ask the Doctor:

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 signs of a serious condition.

Overdosage:
If swallowed, seek medical help or contact a Poison Control Center immediately.

Package Label and Principal Display:

21825297 TRIFLORA 2.75OZCT.jpg

Triflora

Triflora

Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53499-5290
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
COMFREY ROOT COMFREY ROOT 1 [hp_X]
TOXICODENDRON PUBESCENS LEAF TOXICODENDRON PUBESCENS LEAF 3 [hp_X]
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG 1 [hp_X]

Inactive Ingredients

Ingredient Name Strength
CARBOMER HOMOPOLYMER TYPE C
ALCOHOL
pine needle oil (pinus sylvestris)
water
SODIUM HYDROXIDE
WITCH HAZEL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 78 in 1 TUBE
2 28 in 1 TUBE
3 NDC:53499-5290-4 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2006-01-01


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Be sure to consult your doctor before taking any medication!
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