CLEARLIFE EXTRA STRENGTH- onion, galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, sulfur, ambrosia artemisiifolia whole, euphrasia stricta and schoenocaulon officinale seed spray

Clearlife Extra Strength by

Drug Labeling and Warnings

Clearlife Extra Strength by is a Homeopathic medication manufactured, distributed, or labeled by MediNatura Inc., MediNatura Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

*Allium cepa 4X, 12X, 20X, Ambrosia Artemisiaefolia 4X,12X, 20X, Euphrasia Officinalis 4X, 12X, 20X, *Galphimia glauca 4X, 12X, 20X *Histaminum hydrochloricum 8X,12X, 20X, *Luffa operculate 3X,12X, 20X, Sabadilla 4X, 12X, 20X, *Sulphur 4X, 12X, 20X
*Natural Ingredients.

PURPOSE

Relieves:
Runny or itchy Nose
Sneezing
Nasal Congestion
Sinus pressure
Allergic rhinitis
itchy or watery eyes
Allergic related headache

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

For the temporary relief of minor allergy symptoms:Sinus pressure, Runny or itchy nose, Nasal congestion, Allergic rhinitis, sneezing, itchy or watery eyes, Allergic related headache, itchy throat or skin.

WARNINGS

Ask a doctor before use if you have asthma. In rare cases broncho-spasm may occur in asthmatic patients. Temporary burning, stinging, sneezing or increased nasal discharge may occur. If pregnant or breast-feeding, ask a healthcare professional before use. Keep out of reach of children. The use of this dispenser by more than one person may spread infection. If symptoms persist or worsen, a healthcare professional should be consulted. Do not use if known sensitivity to ClearLife™ or any of its ingredients exists.

Directions:

Adults and children 12 years and older: During an allergy attack: 2 sprays into each nostril every 2-4 hours. For daily protection:2 sprays into each nostril daily. Do not exceed 24 sprays in each nostril per 24 hours.
Children 4 to 11 years: During an allergy attack:1 spray into each nostril every 2 to 4 hours. For daily protection 1 spray into each nostril daily. Do not exceed 12 sprays in each nostril per 24 hours.

For children under 4 years, consult your health professional.

INACTIVE INGREDIENTS

Benzalkonium chloride, Disodium phosphate dihydrate, Isotonic sodiumchloride solution, Sodium dihydrogen phosphate dihydrate

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

CLEARLIFE EXTRA STRENGTH 
onion, galphimia glauca flowering top, histamine dihydrochloride, luffa operculata fruit, sulfur, ambrosia artemisiifolia whole, euphrasia stricta and schoenocaulon officinale seed spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62795-4006
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	4 [hp_X]  in 20 mL
GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E)	GALPHIMIA GLAUCA FLOWERING TOP	4 [hp_X]  in 20 mL
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	8 [hp_X]  in 20 mL
LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (LUFFA OPERCULATA FRUIT - UNII:C4MO6809HU)	LUFFA OPERCULATA FRUIT	3 [hp_X]  in 20 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	4 [hp_X]  in 20 mL
AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A)	AMBROSIA ARTEMISIIFOLIA WHOLE	4 [hp_X]  in 20 mL
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	4 [hp_X]  in 20 mL
SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO)	SCHOENOCAULON OFFICINALE SEED	4 [hp_X]  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62795-4006-9	1 in 1 CARTON	01/06/2021
1		20 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/06/2021

Labeler - MediNatura Inc. (079324099)

Establishment
Name	Address	ID/FEI	Business Operations
MediNatura Inc		102783016	manufacture(62795-4006)