Cell Salts description, usages, side effects, indications, overdosage, supplying and lots more!

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Cell Salts

Newton Laboratories, Inc.
Newton Laboratories, Inc.

Cell Salts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

INDICATIONS & USAGE SECTION

Cell Salts     Formulated for mineral balance utilizing all 12 tissue salts.

DOSAGE & ADMINISTRATION SECTION

Directions: ORAL USE ONLY - SHAKE WELL.   Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) one to four times daily or as directed by a healthcare professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Calc. fluor. 10x, Calc. phos. 10x, Calc.sulph. 10x, Ferrum phosphoricum 10x, Kali mur. 10x, Kali phos. 10x, Kali sulph. 10x, Mag. phos. 10x, Nat. mur. 10x, Nat. phos. 10x, Nat.sulphuricum 10x, Silicea 10x.

OTC - PURPOSE SECTION

Formulated for mineral balance utilizing all 12 tissue salts.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.  

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.  

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

Cell Salts

Calc. fluor., Calc. phos., Calc.sulph., Ferrum phosphoricum, Kali mur., Kali phos., Kali sulph., Mag. phos., Nat. mur., Nat. phos., Nat.sulphuricum, Silicea LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55714-2354
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM FLUORIDE Fluoride Ion 10 [hp_X]
TRIBASIC CALCIUM PHOSPHATE CALCIUM CATION 10 [hp_X]
CALCIUM SULFATE ANHYDROUS 10 [hp_X]
FERROSOFERRIC PHOSPHATE Ferrosoferric Phosphate 10 [hp_X]
potassium chloride 10 [hp_X]
potassium phosphate, dibasic PHOSPHATE ION 10 [hp_X]
potassium sulfate 10 [hp_X]
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE MAGNESIUM CATION 10 [hp_X]
SODIUM CHLORIDE 10 [hp_X]
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE SODIUM CATION 10 [hp_X]
SODIUM SULFATE SODIUM CATION 10 [hp_X]
SILICON DIOXIDE 10 [hp_X]

Inactive Ingredients

Ingredient Name Strength
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55714-2354-1 29.57 in 1 BOTTLE, GLASS
2 NDC:55714-2354-2 59.14 in 1 BOTTLE, GLASS
3 NDC:55714-2354-0 .5 in 1 BOTTLE, GLASS

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-03-01


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