Mucus-Clear description, usages, side effects, indications, overdosage, supplying and lots more!

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Mucus-Clear

Native Remedies, LLC

Mucus-Clear




FULL PRESCRIBING INFORMATION

Purpose

Reduce phlegm, mucus and throat congestion

Active ingredient

Active Ingredients: Each dose contains equal parts of: Kali muriaticum 6X HPUS, Kali sulphuricum 6X HPUS, Kali bichromicum 6C HPUS

Uses

Uses: Homeopathic remedy to reduce mucus, phlegm and throat congestion

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 12+: Mix 0.50 mL in 1/4 cup water and sip slowly. Repeat 3-5 times daily as needed until symptoms subside. If preferred, drops may be taken directly into the mouth. Babies and Children under 12 : Reduce dosage to 0.25 mL, 3-5 times daily

Inactive Ingredients: USP Purified water, grain alcohol (20% by volume).

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

All Native Remedies health products are especially 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 animal products, gluten, artificial flavors, preservatives or colorants. Suitable for vegetarians and safe for all ages

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

Mucus-Clear

Mucus-Clear

Kali muriaticum, Kali sulphuricum, Kali bichromicum TINCTURE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68703-089
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POTASSIUM DICHROMATE DICHROMATE ION 6 [hp_X]
potassium chloride 6 [hp_X]
potassium sulfate 6 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68703-089-59 59 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-03-25


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Be sure to consult your doctor before taking any medication!
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