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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

ACETONE: 70 Adverse Event Reports & Safety Profile

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70
Total FAERS Reports
61 (87.1%)
Deaths Reported
8
Hospitalizations
70
As Primary/Secondary Suspect
2
Life-Threatening
Nutritional Specialties, Inc.
Manufacturer

Route: ORAL · Manufacturer: Nutritional Specialties, Inc. · HUMAN OTC DRUG · FDA Label: Available

First Report: 2006 · Latest Report: 20220101

What Are the Most Common ACETONE Side Effects?

#1 Most Reported
Toxicity to various agents
39 reports (55.7%)
#2 Most Reported
Overdose
11 reports (15.7%)
#3 Most Reported
Drug abuse
9 reports (12.9%)

All ACETONE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Toxicity to various agents 39 55.7% 36 2
Overdose 11 15.7% 10 2
Drug abuse 9 12.9% 9 1
Substance abuse 8 11.4% 8 0
Cardiac arrest 6 8.6% 6 1
Chemical poisoning 6 8.6% 6 0
Ketoacidosis 6 8.6% 6 0
Acute kidney injury 5 7.1% 5 2
Cardio-respiratory arrest 5 7.1% 5 1
Death 5 7.1% 5 1
Depressed level of consciousness 5 7.1% 5 2
Hypotension 5 7.1% 5 2
Respiratory depression 5 7.1% 5 2

Who Reports ACETONE Side Effects? Age & Gender Data

Gender: 25.8% female, 74.2% male. Average age: 38.8 years. Most reports from: US. View detailed demographics →

Is ACETONE Getting Safer? Reports by Year

YearReportsDeathsHosp.
2006 1 1 0
2009 1 0 0
2010 1 1 0
2015 1 1 0
2019 2 2 1
2021 4 4 3
2022 1 1 0

View full timeline →

What Is ACETONE Used For?

IndicationReports
Product used for unknown indication 58

Official FDA Label for ACETONE

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

HOMEOPATHIC INDICATIONS: For the temporary relief of symptoms related to petrochemical toxicity including rash, fever, fatigue, headache, muscle and joint pain, and frequent colds.** **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Dosage & Administration

DIRECTIONS: Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. For highly sensitive individuals: best tolerated administration is through imbrication (RUBBING IN) on skin at pulse points or abdomen. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

Warnings

Warnings: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if headache, rash, muscle aches, itching, dizziness, confusion, diarrhea, or other symptoms do not improve within 7 days or are accompanied by fever.

Active Ingredient

ACTIVE INGREDIENTS: Triticum Aestivum 1X, 3X Alfalfa 3X, Arnica Montana 3X, Asclepias Tuberosa 3X, Chamomilla 3X, Echinacea (Angustifolia) 3X, Eucalyptus Globulus 3X, Fucus Vesiculosus 3X, Hordeum Vulgare 3X, Iodium 3X, Nasturtium Aquaticum 3X, Plantago Major 3X, Raphanus Sativus 3X, Trifolium Pratense 3X, Trigonella Foenum-Graecum 3X, Symphytum Officinale 6X, Lung (Suis) 8X, Oryza Sativa 8X, Silicea 8X, Acetone 9X, 12X, 15X, 30X, Sodium Tripolyphosphate 9X, 12X, 15X, 30X, Propylene Glycol 9X, 12X, 15X, 30X, Benzinum 9X, 12X, 15X, 30X, Ammonium Muriaticum 9X, 12X, 15X, 30X, Sodium Lauryl Sulfate 9X, 12X, 15X, 30X, Terebinthina 9X, 12X, 15X, 30X, Arsenicum Album 12X, Natrum Muriaticum 12X, Nitricum Acidum 12X, Phellandrium Aquaticum 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X, Rhus Tox 12X.

Inactive Ingredients

INACTIVE INGREDIENTS: Alcohol USP 20%, Purified Water USP.