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

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Phoenix Balm

Amazonian Naturals, Inc.
Amazonian Naturals, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Camphor 5%.................................... Topical Analgesic
Menthol 5% ..................................... Topical Analgesic
Methyl Salicylate 5%........................ Topical Analgesic

Purposes

Topical Analgesic

Phoenix Balm Uses

For temporary relief of minor aches and pains of muscles and joints associated with over-exertions, arthritis, strains and sprains.

Warnings    For external use only.

When using this product

  • Avoid contact with eyes and mucous membranes.
  • Do not apply to open wounds or damaged skin.
  • Do not bandage or use heating pad.

Stop use and ask a doctor if

  • Condition Worsens.
  • Severe skin irritation occurs.
  • Pain persists for more than seven days.
  • Pain clears up and then recurs a few days later.

If pregnant or breast-feeding ask a health care professional before use.

Keep out of reach of children.  If swallowed get medical help or contact a Poisen Control Center immediately.

Directions

  • Rub well on the affected area.  Repeat 2 or 3 times daily.
  • For children 2 - 12 years, consult a doctor before use.

Other Information

This product may cause allergic reaction in some people.  Test on small area before use.

Inactive Ingredients

Pine needle oil, Cats Claw and Paraffin Petrolatum

Phoenix Balm Phoenix Balm

Phoenix Balm

Pain Relief Rub OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:24438-001
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (NATURAL) 50 mg
MENTHOL 50 mg
methyl salicylate METHYL SALICYLATE 50 mg

Inactive Ingredients

Ingredient Name Strength
pine needle oil (pinus sylvestris)
Cat's Claw
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24438-001-01 19 in 1 CONTAINER
2 NDC:24438-001-02 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-12-01


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Be sure to consult your doctor before taking any medication!
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