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

Menu
Search

Kali bichromicum

Natures Way Holding Co.

Kali bichromicum 30X




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient:

Kali bichromicum 30X

Inactive Ingredients:

Cellulose

Croscarmellose sodium

Lactose

Magnesium stearate

Dosage and Administration:

Boericke and Tafel Brand

Directions: Adults or children over 2 years: Take 3 tablets 1-3 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 (adults) 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.

Pregnancy or Breast Feeding:

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

Keep Out of Reach of Children:

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 (adults) 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 of sinus congestion, pressure or headache.

Package Label and Principal Display:  Boericke and Tafel Brand 21117273

21117273 02 Kali bichromicum 30X 100.jpg

Kali bichromicum

Kali bichromicum

Kali bichromicum TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53499-7272
Route of Administration SUBLINGUAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POTASSIUM DICHROMATE DICHROMATE ION 30 [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:53499-7272-2 100 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!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.