Aspartame MSG Detox description, usages, side effects, indications, overdosage, supplying and lots more!

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Aspartame MSG Detox

Deseret Biologicals, Inc.
Apotheca Company

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS

Chelidonium Majus 3X, Phytolacca Decandra 3X, Arnica Montana 6X, 12X, 30X, 200X, Nitricum Acidum 12X, Nux Vomica 12X, Phosphoricum Acidum 12X, Aspartic Acid​30X, 60X, 200X, Diketopiperazine 30X, 60X, 200X, Dopamine 30X, 60X, 200X, Formalinum 30X, 60X, 200X, Formicum Acidum 30X, 60X, 200X, Methyl Alcohol 30X, 60X, 200X, Monosodium Glutamate 30X, 60X, 200X, Phenylalanine 30X, 60X, 200X,

INDICATIONS

For temporary relief of symptoms related to Aspartame toxicity including headache, dizziness, mood changes, vomiting and nausea, abdominal cramps and pain, vision change, fatigue and weakness and memory loss. 

WARNINGS

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

If pregnant or breast-feeding, seek advice of a health professional before use.

Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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.

INACTIVE INGREDIENTS

Demineralized water, 25% Ethanol.

KEEP OUT OF REACH OF CHILDREN

In case of overdose, contact physician or Poison Control Center right away.

INDICATIONS AND USAGE

For temporary relief of symptoms related to Aspartame toxicity including headache, dizziness, mood changes, vomiting and nausea, abdominal cramps and pain, vision change, fatigue and weakness and memory loss.

QUESTIONS

Dist. By: Deseret Biologicals, Inc.

469 Parkland Drive

Sandy, UT 84070

www.desbio.com

DESBIO

NDC 43742-0215-1

HOMEOPATHIC

ASPARTAME MSG

DETOX

1 FL OZ (30 ml)

Aspartame MSG Detox

Aspartame MSG Detox

Chelidonium Majus, Phytolacca Decandra, Arnica Montana, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:43742-0215
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CHELIDONIUM MAJUS CHELIDONIUM MAJUS 3 [hp_X]
PHYTOLACCA AMERICANA ROOT PHYTOLACCA AMERICANA ROOT 3 [hp_X]
ARNICA MONTANA ARNICA MONTANA 6 [hp_X]
NITRIC ACID NITRIC ACID 12 [hp_X]
STRYCHNOS NUX-VOMICA SEED STRYCHNOS NUX-VOMICA SEED 12 [hp_X]
phosphoric acid PHOSPHORIC ACID 12 [hp_X]
ASPARTIC ACID 30 [hp_X]
2,5-PIPERAZINEDIONE 2,5-PIPERAZINEDIONE 30 [hp_X]
DOPAMINE DOPAMINE 30 [hp_X]
FORMALDEHYDE FORMALDEHYDE 30 [hp_X]
Formic Acid 30 [hp_X]
METHYL ALCOHOL 30 [hp_X]
MONOSODIUM GLUTAMATE 30 [hp_X]
PHENYLALANINE PHENYLALANINE 30 [hp_X]

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43742-0215-1 30 in 1 BOTTLE, DROPPER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2013-04-22


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