N-Con Tonic description, usages, side effects, indications, overdosage, supplying and lots more!

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N-Con Tonic

Native Remedies, LLC

N-Con Tonic




FULL PRESCRIBING INFORMATION

Purpose

Reduce sudden urges and leakages due to incontinence

Active ingredient

Active Ingredients : Each dose contains equal parts of: Calc fluor 6C HPUS, Equisetum arv 3X HPUS, Nat phos 6C HPUS, Nat sulphuricum 6C HPUS, Pulsatilla 3X HPUS.

Uses

Uses: Homeopathic remedy for common incontinence, bladder strength and urinary system support.

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

If pregnant or 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.

Directions: Adults and Children 13+:Take 2 tablets 2-3 times daily as needed. Children 6-12:Take 1-2 tablets 2 times daily as needed. Special instructions: Avoid strong mint flavored candy.

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 produces 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.nativeremedies.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 colors. No gluten added.

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

N-Con Tonic

N-Con Tonic

Calc fluor, Equisetum arv, Nat phos, Nat sulphuricum, Pulsatilla, Acacia gum, lactose, magnesium stearate, corn starch, sucrose TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68703-053
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM FLUORIDE Fluoride Ion 6 [hp_C]
EQUISETUM ARVENSE TOP EQUISETUM ARVENSE TOP 3 [hp_X]
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE SODIUM CATION 6 [hp_C]
SODIUM SULFATE SODIUM CATION 6 [hp_C]
PULSATILLA VULGARIS PULSATILLA VULGARIS 3 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ACACIA
LACTOSE
MAGNESIUM STEARATE
STARCH, CORN
SUCROSE

Product Characteristics

Color Size Shape
white (White lactose tablets) 6 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68703-053-80 180 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-01-16


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Be sure to consult your doctor before taking any medication!
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