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

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DIAMITE

HOMEOLAB USA INC

DRUGS FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients HPUS

Calcarea fluorica, Calcarea phosphorica, Calcarea sulphurica, Ferrum phosphoricum, Kali muriaticum, Kali phosphoricum, Kali sulphuricum, Magnesia phosphorica, Natrum muriaticum, Natrum phosphoricum, Natrum sulphuricum, Silicea 12X

Purpose

...........................................Overall health, general well-being

The letters 'HPUS' indicate that the components in this product are officially monographed in the Homoeopathic Pharmacopoeia of the United States.

DIAMITE Uses

This combination of the 12 tissue salts helps promote overall health and general well-being by replenishing essential minerals.*

*These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.

Warnings

Stop use and ask a doctor if symptoms persist for more than 7 days or worsen.

As with any drug, ask a doctor before use if pregnant or nursing.

Keep this and all medications out of the reach of children.

In case of emergency or accidental overdose, contact a medical professional or a Poison Control Center immediately.

Directions

Children from 2 to 5 years: Crush 2 tablets and dissolve in water 3 times daily, or as directed by a healthcare professional.

Adults and children over 5 years: Chew 2 tablets 3 times daily, or as directed by a healthcare professional.


• Do not use more than directed.

• Do not take with food.

DIAMITE Other information

Store at room temperature.

Do not use if cap seal is broken or missing.

Inactive ingredients

Lactose, magnesium stearate.

LABEL

DIAMITE

DIAMITE

DIAMITE

CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SILICEA TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60512-8036
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM FLUORIDE Fluoride Ion 12 [hp_X]
CALCIUM PHOSPHATE CALCIUM CATION 12 [hp_X]
CALCIUM SULFATE 12 [hp_X]
FERRUM PHOSPHORICUM FERRUM PHOSPHORICUM 12 [hp_X]
potassium chloride 12 [hp_X]
potassium phosphate, dibasic PHOSPHATE ION 12 [hp_X]
potassium sulfate 12 [hp_X]
MAGNESIUM PHOSPHATE, DIBASIC MAGNESIUM PHOSPHATE, DIBASIC 12 [hp_X]
SODIUM CHLORIDE 12 [hp_X]
SODIUM PHOSPHATE, DIBASIC 12 [hp_X]
SODIUM SULFATE SODIUM CATION 12 [hp_X]
SILICON DIOXIDE 12 [hp_X]

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white 8 mm NONE ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60512-8036-5 125 in 1 JAR
2 NDC:60512-8036-6 500 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-03-28


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Be sure to consult your doctor before taking any medication!
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