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

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Kali bichromicum

Natures Way Holding Co.

Kali bichromicum 6X




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient:

Kali bichromicum 6X

Inactive Ingredients:
Cellulose
Croscarmellose sodium
Lactose
Magnesium stearate

Directions:  Adults or children over 2 years: Take 3 tablets 4-6 times a day. 

Allow to dissolve under tongue. 

Stop when symptoms are relieved.

Uses

Indications and Usage:

For the temporary relief of sinus congestion, pressure or headache.

Warnings:

If nasal symptoms do not improve within 7 days or are accompanied by a fever, consult a doctor. 

Do not take this product for pain for more than 10 days (adult) or 5 days (children) unless directed by a doctor. 

If pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor becasue these could be signs of a serious condition.  If pregnant or breast-feeding, ask a healthcare professional before use. 

Pregnancy or Breast Feeding:

If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of reach of children

Ask the Doctor:

If nasal symptoms do not improve within 7 days or are accompanied by a fever, consult a doctor. 

Do not take this product for pain for more than 10 days (adult) or 5 days (children) unless directed by  a doctor. 

If pain persists or gets worse, if new symptoms occur, or if redness or swelling is present, consult a doctor because these could be signs of a serious condition.

Overdosage:

In case of overdose, seek medical help or contact a Poison Control Center immediately.

Purpose

Purpose:

For the temporary relief or sinus congestion, pressure or headache.

Package Label and Principal Display: Boericke and Tafel Breand 21117233

21117233 02 Kali bichromicum 6X 100.jpg

Kali bichromicum

Kali bichromicum

Kali bichromicum TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53499-7233
Route of Administration SUBLINGUAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POTASSIUM DICHROMATE DICHROMATE ION 6 [hp_X]

Inactive Ingredients

Ingredient Name Strength
cellulose, microcrystalline
LACTOSE
MAGNESIUM STEARATE
CROSCARMELLOSE SODIUM

Product Characteristics

Color Size Imprint Code Shape
white (white tablet) 6 mm B;T ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53499-7233-2 100 in 1 BOTTLE, GLASS

Marketing Information

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


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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