SINUSITIS (pulsatilla- vulgaris, plantago major, euphorbium officinarum, luffa operculata, mercurius iodatus ruber, mucosa nasalis suis, argentum nitricum, hepar sulphuris calcareum, calcarea carbonica, natrum muriaticum, sinusitisinum liquid

Sinusitis by

Drug Labeling and Warnings

Sinusitis by is a Homeopathic medication manufactured, distributed, or labeled by Deseret Biologicals, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Pulsatilla (Vulgaris) 1X, Plantago Major 3X, Luffa Operculata 6X, Mercurius Iodatus Ruber 8X, Mucosa Nasalis Suis 8X, Euphorbium Officinarum 9X, Argentum Nitricum 10X, Hepar Sulphuris Calcareum 10X, Calcarea Carbonica 12X, Natrum Muriaticum 12X, Sinusitisinum 20X.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms of acute and chronic sinusitis.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

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

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.

HOMEOPATHIC INDICATIONS:

For temporary relief of symptoms of acute and chronic sinusitis.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070   www.desbio.com

PACKAGE LABEL DISPLAY:

DESBIO

NDC: 43742-1005-1

HOMEOPATHIC

SINUSITIS

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

SINUSITIS 
pulsatilla (vulgaris), plantago major, euphorbium officinarum, luffa operculata, mercurius iodatus ruber, mucosa nasalis suis, argentum nitricum, hepar sulphuris calcareum, calcarea carbonica, natrum muriaticum, sinusitisinum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43742-1005
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PULSATILLA VULGARIS (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV)	PULSATILLA VULGARIS	1 [hp_X]  in 1 mL
PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U)	PLANTAGO MAJOR	3 [hp_X]  in 1 mL
LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU)	LUFFA OPERCULATA FRUIT	3 [hp_X]  in 1 mL
MERCURIC IODIDE (UNII: R03O05RB0P) (MERCURIC IODIDE - UNII:R03O05RB0P)	MERCURIC IODIDE	6 [hp_X]  in 1 mL
SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY)	SUS SCROFA NASAL MUCOSA	8 [hp_X]  in 1 mL
EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K)	EUPHORBIA RESINIFERA RESIN	8 [hp_X]  in 1 mL
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	9 [hp_X]  in 1 mL
CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q)	CALCIUM SULFIDE	10 [hp_X]  in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I)	OYSTER SHELL CALCIUM CARBONATE, CRUDE	10 [hp_X]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	12 [hp_X]  in 1 mL
SINUSITISINUM (UNII: B575563DM5) (SINUSITISINUM - UNII:B575563DM5)	SINUSITISINUM	20 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43742-1005-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/02/2017	02/12/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/02/2017	02/12/2023

Labeler - Deseret Biologicals, Inc. (940741853)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43742-1005) , api manufacture(43742-1005) , label(43742-1005) , pack(43742-1005)