FDA.reportPublic FDA data

ChemDetox

Manufacturer
Dr. Donna Restivo DC | Apotheca Company
Effective date
2024-01-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:13:56

Label at a glance#

ProductChemDetox
Active ingredientBERBERIS VULGARIS ROOT BARK, GLYCYRRHIZA GLABRA, ARCTIUM LAPPA ROOT, STILLINGIA SYLVATICA ROOT, TRIFOLIUM PRATENSE FLOWER, SUS SCROFA ADRENAL GLAND, PORK LIVER, SUS SCROFA LYMPH, PHYTOLACCA AMERICANA ROOT, SUS SCROFA THYROID, IRIDIUM, LYCOPODIUM CLAVATUM SPORE, NITRIC ACID, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, SELENIUM, SALICYLIC ACID, CORTICOTROPIN, CORTISONE ACETATE, EUGENOL, STEARYL ALCOHOL, XYLITOL, ESTRONE, BENZOIC ACID, CHLORINE, POTASSIUM SORBATE, SORBITOL, RESORCINOL, BENZYL ALCOHOL, LACTIC ACID, DL-, ISOPROPYL PALMITATE, BORIC ACID, ACETIC ACID, PHENYL BUTYRATE, PETROLATUM, LEAD
Label structure9 sections

Dosage and administration

10 drops under the tongue, 3 to 6 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Berberis Vulgaris 3X, Glycyrrhiza Glabra 3X, Lappa Major 3X, Stillingia Sylvatica 3X, Trifolium Pratense 3X, Glandula Suprarenalis Suis 8X, Hepar Suis 8X, Lymph (Suis) 8X, Phytolacca Decandra 8X, Thyroidinum (Suis) 8X, Iridium Metallicum 12X, Lycopodium Clavatum 12X, Nitricum Acidum 12X, Nux Vomica 12X, Phosphoricum Acidum 12X, Selenium Metallicum 12X, Salicylicum Acidum 30X, 60X, 200X, Adrenocorticotrophin 30X, 60X, 200X, Cortisone Aceticum 30X, 60X, 200X, Eugenol 30X, 60X, 200X, Stearyl Alcohol 30X, 60X, 200X, Xylitol 30X, 60X, 200X, Folliculinum 30X, 60X, 200X, Benzoicum Acidum 30X, 60X, 200X, Chlorinum 30X, 60X, 200X, Potassium Sorbate 30X, 60X, 200X, Sorbitol 30X, 60X, 200X, Resorcinum 30X, 60X, 200X, Benzyl Alcohol 30X, 60X, 200X, Lacticum Acidum 30X, 60X, 200X, Isopropyl Palmitate 30X, 60X, 200X, Boricum Acidum 30X, 60X, 200X, Aceticum Acidum 30X, 60X, 200X, Phenyl Butazone 30X, 60X, 200X, Petroleum Jelly 30X, 60X, 200X, Plumbum Metallicum 30X, 60X, 200X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to chemical toxicity including fatigue, frequent colds, insomnia, headache, rash, occasional constipation, and memory difficulties.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Tamper seal: Sealed for your protection.

Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops under the tongue, 3 to 6 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to chemical toxicity including fatigue, frequent colds, insomnia, headache, rash, occasional constipation, and memory difficulties.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

demineralized water, 25% ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by Dr. Donna Restivo DC, Wellness Consultant

822 South Lake Blvd. Mahopac, New York 10541

www.mahopacmassage.com • (845) 628-6286

*For a complete list of Chemical Isodes contact Dr. Donna Restivo DC, Wellness Consultant.

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR. DONNA RESTIVO DC

WELLNESS CONSULTANT

NDC 62185-0012-1

HOMEOPATHIC

ChemDETOX

1 FL OZ (30 ml)

ChemDetoxChemDetox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62185-0035-12024-01-18C16284748780-19d75b9d0-8f47-f424-e053-dadaa90a57ceDrug Facts:
62185-0035-12020-01-31C16284748780-19d75b9d0-8f47-f424-e053-dadaa90a57ceDrug Facts:

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62185-003562185-0035-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
GLYCYRRHIZA GLABRA2788Z9758HACTIB
ARCTIUM LAPPA ROOT597E9BI3Z3ACTIB
STILLINGIA SYLVATICA ROOTQBR70R4FBKACTIB
TRIFOLIUM PRATENSE FLOWER4JS0838828ACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
PORK LIVER6EC706HI7FACTIB
SUS SCROFA LYMPH33A7VYU29LACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
SUS SCROFA THYROID6RV024OAUQACTIB
IRIDIUM44448S9773ACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
NITRIC ACID411VRN1TV4ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
SELENIUMH6241UJ22BACTIB
SALICYLIC ACIDO414PZ4LPZACTIB
CORTICOTROPINK0U68Q2TXAACTIB
CORTISONE ACETATE883WKN7W8XACTIB
EUGENOL3T8H1794QWACTIB
STEARYL ALCOHOL2KR89I4H1YACTIB
XYLITOLVCQ006KQ1EACTIB
ESTRONE2DI9HA706AACTIB
BENZOIC ACID8SKN0B0MIMACTIB
CHLORINE4R7X1O2820ACTIB
POTASSIUM SORBATE1VPU26JZZ4ACTIB
SORBITOL506T60A25RACTIB
RESORCINOLYUL4LO94HKACTIB
BENZYL ALCOHOLLKG8494WBHACTIB
LACTIC ACID, DL-3B8D35Y7S4ACTIB
ISOPROPYL PALMITATE8CRQ2TH63MACTIB
BORIC ACIDR57ZHV85D4ACTIB
ACETIC ACIDQ40Q9N063PACTIB
PHENYL BUTYRATER9K49A127HACTIB
PETROLATUM4T6H12BN9UACTIB
LEAD2P299V784PACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ce7faf05-26b1-4131-93ad-df23316bf01f490d57de-d9f3-4335-ab62-401510133b832024-01-18WarningsExact identifier
spl id: ce7faf05-26b1-4131-93ad-df23316bf01f
spl set id: 490d57de-d9f3-4335-ab62-401510133b83

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.