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

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Acne Clear

King Bio Inc.
King Bio Inc.

Acne Clear™




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts​__________________________________________________________________________________________________________

HPUS active ingredients: ​Antimonium tartaricum, Asterias rubens, Ferrum metallicum, Hepar sulphuris calcareum, Kali bromatum, Natrum muriaticum, Sanguinaria canadensis, Selenium metallicum, Sepia, Silica, Sulphur, Thuja occidentalis. Equal volumes of each ingredient in 10X, 30X, 100X, 1M, LM1, LM2, LM3 potencies.

Uses

Uses for temporary relief from acne symptoms: pimples, blackheads, oily skin, skin eruptions, unhealthy skin, teenage and adult acne, skin inflammation, uneven skin tone, and menstrual breakouts.

Inactive Ingredients:

Bio-Energetically Enhanced™ pure water, citric acid and 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 seal is intact. This product has not been independently tested.

Purpose

Uses for temporary relief from acne symptoms:

  • pimples
  • blackheads
  • oily skin
  • skin eruptions
  • unhealthy skin
  • teenage and adult acne
  • skin inflammation
  • uneven skin tone
  • menstrual breakouts

Acne Clear

Acne Clear

Antimonium tartaricum, Asterias rubens, Ferrum metallicum, Hepar sulphuris calcareum, Kali bromatum, Natrum muriaticum, Sanguinaria canadensis, Selenium metallicum, Sepia, Silica, Sulphur, Thuja occidentalis LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57955-0041
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Antimony Potassium Tartrate ANTIMONY CATION (3+) 10 [hp_X]
Asterias Rubens ASTERIAS RUBENS 10 [hp_X]
IRON IRON 10 [hp_X]
CALCIUM SULFIDE CALCIUM CATION 10 [hp_X]
POTASSIUM BROMIDE POTASSIUM CATION 10 [hp_X]
SODIUM CHLORIDE 10 [hp_X]
SANGUINARIA CANADENSIS ROOT SANGUINARIA CANADENSIS ROOT 10 [hp_X]
Selenium SELENIUM 10 [hp_X]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE 10 [hp_X]
SILICON DIOXIDE 10 [hp_X]
SULFUR SULFUR 10 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 10 [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:57955-0041-2 59 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-05-21


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