Lungs and Bronchial Relief

LUNGS AND BRONCHIAL RELIEF- ammonium carbonicum, antimonium arsenicicum, antimonium tartaricum, arsenicum album, bromium, carbo vegetabilis, chlorinum, kali carbonicum, lobelia inflata, stannum metallicum, sulphuricum acidum liquid
New Sun Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Directions: Before initial dose depress pump 4-5 times or until primed and spray 1 dose directly in mouth 4 to 6 times daily until symptoms improve.

Adult Dose: 3 Pump Sprays

Child's Dose (2-12): 2 Pump Sprays

Infants - 2 yrs: 1 Pump Spray

Warnings:If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, take only on advice of physician.

Keep out of reach of children.

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

Indications: For temporary relief of: •shortness of breath •tightness in chest •wheezing •upper respiratory/bronchial congestion & cough •mucus congestion •symptoms of emphysema pain in chest

Active Ingredients: Ammonium carbonicum, Antimonium arsenicicum, Antimonium tartaricum, Arsenicum album, Bromium, Carbo vegetabilis, Chlorinum, Kali carbonicum, Lobelia inflata, Stannum metallicum, Sulphuricum acidum. Equal volumes of each ingredient in 10X, 30X, and 100X potencies.

Inactive Ingredient: Citric acid, potassium sorbate, purified water.

Indications: For temporary relief of:

shortness of breath
tightness in chest
wheezing
upper respiratory/bronchial congestion & cough
mucus congestion
symptoms of emphysema pain in chest

image description

LUNGS AND BRONCHIAL RELIEF
ammonium carbonicum, antimonium arsenicicum, antimonium tartaricum, arsenicum album, bromium, carbo vegetabilis, chlorinum, kali carbonicum, lobelia inflata, stannum metallicum, sulphuricum acidum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66579-0067
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CARBONATE	10 [hp_X] in 59 mL
ANTIMONY ARSENATE (UNII: WE3458XNFT) (ARSENATE ION - UNII:G1DBI405OK)	ANTIMONY ARSENATE	10 [hp_X] in 59 mL
ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3) (ANTIMONY CATION (3+) - UNII:069647RPT5)	ANTIMONY POTASSIUM TARTRATE	10 [hp_X] in 59 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	10 [hp_X] in 59 mL
BROMINE (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G)	BROMINE	10 [hp_X] in 59 mL
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	10 [hp_X] in 59 mL
CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820)	CHLORINE	10 [hp_X] in 59 mL
POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D)	POTASSIUM CARBONATE	10 [hp_X] in 59 mL
LOBELIA INFLATA (UNII: 9PP1T3TC5U) (LOBELIA INFLATA - UNII:9PP1T3TC5U)	LOBELIA INFLATA	10 [hp_X] in 59 mL
TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5)	TIN	10 [hp_X] in 59 mL
SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF)	SULFURIC ACID	10 [hp_X] in 59 mL

Ingredient Name	Strength
Inactive Ingredients
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66579-0067-2	59 mL in 1 BOTTLE, SPRAY

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/17/2014

Labeler - New Sun Inc. (957251176)

Registrant - New Sun Inc. (957251176)