Environmental Adaptation Cold and Dry description, usages, side effects, indications, overdosage, supplying and lots more!

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Environmental Adaptation Cold and Dry

King Bio Inc.
King Bio Inc.

Environmental Adaptation Cold and Dry




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts

____________________________________________________________________________________________________________________

HPUS active ingredients: ​Aconitum napellus, Agaricus muscarius, Asarum europaeum, Aurum metallicum, Bryonia, Camphora, Causticum, Hepar sulphuris calcareum, Hypothalamus, Kali carbonicum, Petroleum, Secale cornutum, Sepia, Thyroidinum. Equal volumes of each ingredient in 10X, 30X, 100X, LM1, LM2, LM3, LM5 potencies.

Uses

Uses ​for temporary relief of: cold, dry environments: cold, numb and stiff extremities, cough, hoarseness, dry nose, lips, difficult respiration, teeth and head pain, blotchy skin, fatigue.

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: 3 sprays 3 times per day.
  • Children 2-12 years: 2 sprays 3 times per day.
  • Use additionally as needed, up to 6 times per day.

Tamper resistant for your protection. Use only if safety seal is intact.

Purpose

Uses for temporary relief of: cold, dry environments:

  • cold, numb and stiff extremities
  • cough
  • hoarseness
  • dry nose
  • lips
  • difficult respiration
  • teeth and head pain
  • blotchy skin
  • fatigue

Environmental Adaptation Cold and Dry

Environmental Adaptation Cold and Dry

Aconitum napellus, Agaricus muscarius, Asarum europaeum, Aurum metallicum, Bryonia, Camphora, Causticum, Hepar sulphuris calcareum, Hypothalamus, Kali carbonicum, Petroleum, Secale cornutum, Sepia, Thyroidinum LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57955-0288
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACONITUM NAPELLUS ACONITUM NAPELLUS 10 [hp_X]
AMANITA MUSCARIA FRUITING BODY AMANITA MUSCARIA FRUITING BODY 10 [hp_X]
ASARUM EUROPAEUM ASARUM EUROPAEUM 10 [hp_X]
GOLD 10 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 10 [hp_X]
CAMPHOR (NATURAL) 10 [hp_X]
CAUSTICUM CAUSTICUM 10 [hp_X]
CALCIUM SULFIDE CALCIUM CATION 10 [hp_X]
BOS TAURUS HYPOTHALAMUS BOS TAURUS HYPOTHALAMUS 10 [hp_X]
POTASSIUM CARBONATE CARBONATE ION 10 [hp_X]
KEROSENE KEROSENE 10 [hp_X]
CLAVICEPS PURPUREA SCLEROTIUM CLAVICEPS PURPUREA SCLEROTIUM 10 [hp_X]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE 10 [hp_X]
THYROID, UNSPECIFIED THYROID, UNSPECIFIED 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:57955-0288-2 59 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-04-17


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