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

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HaliTonic

Native Remedies LLC

HaliTonic




FULL PRESCRIBING INFORMATION

Purpose

Temporary relief from bad breath and halitosis

Active ingredient

Active Ingredients: Each tablet contains equal part of: Carduus mar 3X HPUS, Kali phos 6C HPUS, Nat sulphuricum 6C HPUS, Nux vom 3X HPUS, Silicea 6C HPUS.

Uses

Uses: Homeopathic remedy for breath freshness and halitosis.

Warnings: If symptoms persist or worsen, consult a healthcare professional.

If pregnant of breastfeeding, ask a health professional before use.

Keep this and all medication out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. Not recommended for those with surgical implants or prostheses unless under medical supervision.

Directions: For all ages: Dissolve 2 tablets directly in the mouth 2-4 times daily. Alternatively, for small babies, crush tablets and sprinkle onto tongue.

Inactive Ingredients: Acacia gum, lactose,magnesium stearate, corn starch, sucrose.

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

All Native Remedies health products are specially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.natiremedies.com

Distributed by
Native Remedies, LLC
6531 Park of Commerce Blvd.
Suite 160
Boca Raton, Fl 33487
Phone:+1.877.289.1235
International:+1.561.999.8857

Contains no artificial flavors or artificial color. No gluten added.

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

HaliTonic

HaliTonic

Carduus mar, Kali phos, Nat sulphuricum, Nux vom, Silicea, Acacia gum, Lactose, Magnesium stearate, Corn starch, Sucrose. TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68703-006
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SILYBUM MARIANUM SEED SILYBUM MARIANUM SEED 3 [hp_X]
potassium phosphate, dibasic PHOSPHATE ION 6 [hp_C]
SODIUM SULFATE SODIUM CATION 6 [hp_C]
STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED 3 [hp_X]
SILICON DIOXIDE 6 [hp_C]

Inactive Ingredients

Ingredient Name Strength
ACACIA
LACTOSE
MAGNESIUM STEARATE
STARCH, CORN
SUCROSE

Product Characteristics

Color Size Shape
white (white lactose tablet) 6 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68703-006-80 180 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-12-28


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Be sure to consult your doctor before taking any medication!
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