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Sinusitis Plus

Deseret Biologicals, Inc.
Apotheca Company

Sinusitis Plus




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:  Kali muriaticum 6X, 200C, Calcarea sulphurica 10X, 200C, Sulphur 6C, Mucor racemosus 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, 200C, Aspergillus niger 10C, 15C, 30C, 200C, Candida albicans 10C, 15C, 30C, 200C, Thuja occidentalis 12C, 200C, Sinusitisinum 15C.

Purpose

INDICATIONS:  For the relief of symptoms of acute and chronic sinusitis.

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

If pregnant or breast-feeding, seek advice of a health professional before use.

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

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

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, contact physician or Poison Control Center right away.

Uses

INDICATIONS:  For the relief of symptoms of acute and chronic Sinusitis.

Dist. By:

Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com


DESBIO

NDC 43742-0034-1

HOMEOPATHIC

SINUSITIS PLUS

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, Hepar sulphuris calcareum, Argentum nitricum, Cobaltum metallicum, Cuprum metallicum, Manganum metallicum, Silicea, Aspergillus fumigatus, LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0034
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
ALCOHOL
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0034-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-05-16


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