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Cataracts

Newton Laboratories, Inc.
Newton Laboratories, Inc.

Cataracts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

  Catatacts   Formulated for symptoms associated with cataracts such as blurred vision, photophobia, diplopia and opacities.         

DOSAGE & ADMINISTRATION SECTION

Directions:  Ages 12 and up, take 6 pellets orally one to four times daily or as directed by a healthcare professional.      

ACTIVE INGREDIENT SECTION

Arsenicum alb. 15x, Bryonia 15x, Calc. fluor. 15x, Calendula 15x, Causticum 15x, Conium  15x, Euphrasia 15x, Hydrofluoricum acidum  15x, Iodium 15x, Ledum 15x, Naphthalinum 15x, Nat. mur. 15x, Nux vom. 15x, Phosphorus 15x, Pulsatilla 15x, Sepia 15x, Silicea 15x, Tellurium metallicum 15x, Thiosinaminum 15x, Zinc. met. 15x, Euphrasia 3x.       

PURPOSE SECTION

Formulated for symptoms associated with cataracts such as blurred vision, photophobia, diplopia and opacities.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Gluten-free, non-GMO, beet-derived sucrose pellets.                  

QUESTIONS? SECTION

www.newtonlabs.net   Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions?  1.800.448.7256         

WARNINGS SECTION

Warning:  Do not use if tamper - evident seal is broken or missing.  Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.  Keep out of reach of children.        

PREGNANCY OR BREAST FEEDING SECTION

Consult a licensed healthcare professional if pregnant or nursing or if symptoms worsen or persist for more than a few days.              

KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.            

PACKAGE LABEL

Cataracts

Arsenicum alb., Bryonia, Calc. fluor., Calendula, Causticum, Conium , Euphrasia, Hydrofluoricum acidum, Iodium, Ledum, Naphthalinum, Nat. mur., Nux vom., Phosphorus, Pulsatilla, Sepia, Silicea, Tellurium metallicum, Thiosinaminum, Zinc. met. PELLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:55714-4589
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ARSENIC TRIOXIDE ARSENIC TRIOXIDE 15 [hp_X]
BRYONIA ALBA ROOT BRYONIA ALBA ROOT 15 [hp_X]
CALCIUM FLUORIDE Fluoride Ion 15 [hp_X]
CALENDULA OFFICINALIS FLOWERING TOP CALENDULA OFFICINALIS FLOWERING TOP 15 [hp_X]
CAUSTICUM CAUSTICUM 15 [hp_X]
Conium Maculatum Flowering Top CONIUM MACULATUM FLOWERING TOP 15 [hp_X]
EUPHRASIA STRICTA EUPHRASIA STRICTA 15 [hp_X]
Hydrofluoric Acid Hydrofluoric Acid 15 [hp_X]
Iodine IODINE 15 [hp_X]
LEDUM PALUSTRE TWIG LEDUM PALUSTRE TWIG 15 [hp_X]
Naphthalene Naphthalene 15 [hp_X]
SODIUM CHLORIDE 15 [hp_X]
STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED 15 [hp_X]
PHOSPHORUS PHOSPHORUS 15 [hp_X]
PULSATILLA VULGARIS PULSATILLA VULGARIS 15 [hp_X]
SEPIA OFFICINALIS JUICE SEPIA OFFICINALIS JUICE 15 [hp_X]
SILICON DIOXIDE 15 [hp_X]
Tellurium Tellurium 15 [hp_X]
Allylthiourea ALLYLTHIOUREA 15 [hp_X]
Zinc ZINC 15 [hp_X]

Inactive Ingredients

Ingredient Name Strength
SUCROSE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55714-4589-1 28.35 in 1 BOTTLE, GLASS
2 NDC:55714-4589-2 56.7 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-06-01


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