DIAMITE 12- 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

DIAMITE 12 by

Drug Labeling and Warnings

DIAMITE 12 by is a Homeopathic medication manufactured, distributed, or labeled by HOMEOLAB USA INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients HPUS

Calcarea fluorica 6X, Calcarea phosphorica 6X, Calcarea sulphurica 6X, Ferrum phosphoricum 5X, Kali muriaticum 4X, Kali phosphoricum 3X, Kali sulphuricum 6X, Magnesia phosphorica 3X, Natrum muriaticum 6X, Natrum phosphoricum 3X, Natrum sulphuricum 3X, Silicea 6X

Purpose

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

REFERENCES

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

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.

Other information

Store at room temperature.

Do not use if film wrapper is damaged or missing.

Inactive ingredients

Lactose, magnesium stearate.

LABEL

INGREDIENTS AND APPEARANCE

DIAMITE 12 
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	Item Code (Source)	NDC: 60512-8037
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM FLUORIDE (UNII: O3B55K4YKI) (FLUORIDE ION - UNII:Q80VPU408O)	CALCIUM FLUORIDE	6 [hp_X]
CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM PHOSPHATE	6 [hp_X]
CALCIUM SULFATE (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE	6 [hp_X]
FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7)	FERRUM PHOSPHORICUM	5 [hp_X]
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	4 [hp_X]
POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR)	POTASSIUM PHOSPHATE, DIBASIC	3 [hp_X]
POTASSIUM SULFATE (UNII: 1K573LC5TV) (SULFATE ION - UNII:7IS9N8KPMG)	POTASSIUM SULFATE	6 [hp_X]
MAGNESIUM PHOSPHATE, DIBASIC (UNII: A1Y870209Z) (MAGNESIUM PHOSPHATE, DIBASIC - UNII:A1Y870209Z)	MAGNESIUM PHOSPHATE, DIBASIC	3 [hp_X]
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	6 [hp_X]
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) (PHOSPHATE ION - UNII:NK08V8K8HR)	SODIUM PHOSPHATE, DIBASIC	3 [hp_X]
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)	SODIUM SULFATE	3 [hp_X]
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (COLLOIDAL SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	NONE
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60512-8037-7	5000 in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/12/2015

Labeler - HOMEOLAB USA INC (202032533)

Establishment
Name	Address	ID/FEI	Business Operations
HOMEOLAB USA INC		202032533	manufacture(60512-8037)