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Advanced Arnica

King Bio Inc.
King Bio Inc.

Advanced Arnica




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts

____________________________________________________________________________________________________________________

HPUS active ingredients: Arnica montana, Arnica montana, radix . Equal volumes of each ingredient in 6X, 30X, 6C, 30C, LM1, LM2, LM3 potencies.

Uses

Uses​ temporarily relieves symptoms due to injury or overexertion: bruises, muscle pain, inflammation, body aches, sprains, traumatic injury, redness and swelling, soreness after exercise, rheumatic pain.

Inactive ingredients: Bio-Energetically Enhanced pure water, citric acid, potassium sorbate.

Warnings

  • Stop use and ask your doctor if symptoms persist or worsen.
  • If pregnant or breast-feeding, take only on advice of a healthcare professional.

  • Keep out of reach of children.

Directions:

  • Initially, depress pump until primed.
  • Spray one dose directly into mouth.
  • Adults 12 and up: 3 sprays 3 times per day.
  • Children 2-12 : 2 sprays 3 times per day.
  • Children 2 mo-2 yr: 1 spray 3 times per day.

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been independently tested.

Purpose

Uses temporarily relieves symptoms due to injury or overexertion:

  • bruises
  • muscle pain
  • inflammation
  • body aches
  • sprains
  • traumatic injury
  • redness and swelling
  • soreness after exercise
  • rheumatic pain

Advanced Arnica

Advanced Arnica

Arnica montana, Arnica montana, radix LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57955-7304
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARNICA MONTANA ARNICA MONTANA 6 [hp_X]
ARNICA MONTANA ROOT ARNICA MONTANA ROOT 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57955-7304-2 59 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-12-17


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