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Sinusitis Plus

Deseret Biologicals, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS:


Kali muriaticum 6X, 200C, Calcarea sulphurica 10X, 200C, Sulphur 6C, Mucor racemousus 6C, 15C, 30C, 200C, Hydrastis canadensis 7C, 200C, Kali bichromicum 7C, 200C, Lachesis mutus 7C, 200C, Mercurius sulphuratus ruber 7C, 200C, Hepar sulphuris calcareum 7C, 10C, 200C, Argentum nitricum 10C, Cobaltum metallicum 10C, Cuprum metallicum 10C, Manganum metallicum 10C, Silicea 10C, Aspergillus fumigatus 10C, 15C, 30C, 200C, Aspergillus niger 10C, 15C, 30C, 200C, Candida albicans 10C, 15C, 30C, 200C, Thuja occidentalis 12C, 200C, Sinusitisinum 15C.

INDICATIONS:

For temporary relief of symptoms related to ear, nose and throat infections including sinus/nasal congestion, cough, and mucous congestion in the middle ear, sneezing, and vaccination reaction.

WARNINGS:

Keep out of reach of children.  In case of overdose, contact a physician or Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: "Sealed for Your Protection."  Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children.  In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

1-10 drops under the tongue, 3 times a day or as directed by a health profressional.  Consult a physician for use in children under 12 years of age.

INDICATIONS:

For temporary relief of symptoms related to ear, nose and throat infections including sinus/nasal congestion, cough, and mucous congestion in the middle ear, sneezing, and vaccination reaction.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol.

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070     www.desbio.com

PACKAGE LABEL DISPLAY

DESBIO

NDC 43742-0375-1

HOMEOPATHIC

SINUSITIS PLUS

(with ENT Support)

1 FL OZ (30 ml)

Sinusitis Plus

Sinusitis Plus

Kali muriaticum, Calcarea sulphurica, Sulphur, Mucor racemosus, Hydrastis canadensis, Kali bichromicum, Lachesis mutus, Mercurius sulphuratus ruber, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0375
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
potassium chloride 6 [hp_X]
CALCIUM SULFATE ANHYDROUS 10 [hp_X]
SULFUR SULFUR 6 [hp_C]
MUCOR RACEMOSUS mucor racemosus 6 [hp_C]
GOLDENSEAL GOLDENSEAL 7 [hp_C]
POTASSIUM DICHROMATE DICHROMATE ION 7 [hp_C]
LACHESIS MUTA VENOM LACHESIS MUTA VENOM 7 [hp_C]
Mercuric Sulfide MERCURIC CATION 7 [hp_C]
CALCIUM SULFIDE CALCIUM CATION 7 [hp_C]
SILVER NITRATE SILVER CATION 10 [hp_C]
COBALT Cobalt 10 [hp_C]
Copper COPPER 10 [hp_C]
MANGANESE Manganese 10 [hp_C]
SILICON DIOXIDE 10 [hp_C]
ASPERGILLUS FUMIGATUS ASPERGILLUS FUMIGATUS 10 [hp_C]
ASPERGILLUS NIGER VAR. NIGER Aspergillus Niger Var. Niger 10 [hp_C]
CANDIDA ALBICANS candida albicans 10 [hp_C]
THUJA OCCIDENTALIS LEAFY TWIG THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_C]
SINUSITISINUM SINUSITISINUM 15 [hp_C]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0375-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2014-04-28


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Be sure to consult your doctor before taking any medication!
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