FDA.reportPublic FDA data

Intercellular Detox

Manufacturer
Dr. Donna Restivo DC | Apotheca Company
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:21:22

Label at a glance#

ProductIntercellular Detox
Active ingredientCEANOTHUS AMERICANUS LEAF, SEMECARPUS ANACARDIUM JUICE, SILVER NITRATE, MARSDENIA CONDURANGO BARK, GOLDENSEAL, MOMORDICA BALSAMINA IMMATURE FRUIT, OXALIS ACETOSELLA LEAF, ANEMONE PULSATILLA, SUS SCROFA BILE DUCT, SUS SCROFA COLON, SUS SCROFA DUODENUM, SUS SCROFA ESOPHAGUS, SUS SCROFA EYE, SUS SCROFA GALLBLADDER, SUS SCROFA ILEUM, PORK INTESTINE, IPECAC, SUS SCROFA JEJUNUM, POTASSIUM DICHROMATE, SUS SCROFA LUNG, SUS SCROFA NASAL MUCOSA, SODIUM DIETHYL OXALACETATE, SUS SCROFA ORAL MUCOSA, SUS SCROFA PANCREAS, PHOSPHORUS, SUS SCROFA RECTAL MUCOSA, SUS SCROFA STOMACH, SULFUR, VERATRUM ALBUM ROOT, YEAST MANNAN, WOOD CREOSOTE, LACHESIS MUTA VENOM, MANDRAGORA OFFICINARUM ROOT, SUS SCROFA URINARY BLADDER, SHIGELLA DYSENTERIAE
Label structure9 sections

Dosage and administration

10 drops under the tongue, 3 to 6 times per 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

Ceanothus Americanus 4X, Veratrum Album 4X, Anacardium Orientale 6X, Argentum Nitricum 6X, Condurango 6X, Hydrastis Canadensis 6X, Momordica Balsamina 6X, Oxalis Acetosella 6X, Pulsatilla (Vulgaris) 6X, Bile Duct (Suis) 8X, Colon (Suis) 8X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Eye (Suis) 8X, Gallbladder (Suis) 8X, Ileum (Suis) 8X, Intestine (Suis) 8X, Ipecacuanha 8X, Jejunum (Suis) 8X, Kali Bichromicum 8X, Lung (Suis) 8X, Mucosa Nasalis Suis 8X, Natrum Oxalaceticum 8X, Oral Mucosa (Suis) 8X, Pancreas Suis 8X, Phosphorus 8X, Rectal Mucosa (Suis) 8X, Stomach (Suis) 8X, Sulphur 8X, Mannan 8X, 30X, 200X, Kreosotum 10X, Lachesis Mutus 10X, Mandragora Officinarum 10X, Urinary Bladder (Suis) 6C, Dysentery Bacillus 30C, 200C.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.**

**These statements are based upon traditional 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 or 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 or a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops under the tongue, 3 to 6 times per 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 such as occasional diarrhea, occasional constipation, headaches, gas, congestion, irritated eyes, and indigestion.**

**These statements are based upon traditional 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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR. DONNA RESTIVO DC
WELLNESS CONSULTANT
NDC 62185-0039-1
HOMEOPATHIC
Intercellular DETOX
1 FL OZ (30 ml)

Intercellular DetoxIntercellular Detox

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62185-0044-12021-12-23C16284748780-1ba0f9c33-25bd-a910-e053-dadaa90a0b85Drug Facts:
62185-0044-12021-01-29C16284748780-1ba0f9c33-25bd-a910-e053-dadaa90a0b85Drug 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
62185-004462185-0044-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
CEANOTHUS AMERICANUS LEAF25B1Y14T8NACTIB
SEMECARPUS ANACARDIUM JUICEY0F0BU8RDUACTIB
SILVER NITRATE95IT3W8JZEACTIB
MARSDENIA CONDURANGO BARKR23QIR6YBAACTIB
GOLDENSEALZW3Z11D0JVACTIB
MOMORDICA BALSAMINA IMMATURE FRUITWUW1665V10ACTIB
OXALIS ACETOSELLA LEAFU1W3U02EW0ACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
SUS SCROFA BILE DUCT4EE983392UACTIB
SUS SCROFA COLON94J255A0UCACTIB
SUS SCROFA DUODENUMP6J2SFT80OACTIB
SUS SCROFA ESOPHAGUS81FZ7X4MWDACTIB
SUS SCROFA EYEX3AOK514E6ACTIB
SUS SCROFA GALLBLADDERB6A98VOI9IACTIB
SUS SCROFA ILEUMC998R1XSRAACTIB
PORK INTESTINE40GMI0R60LACTIB
IPECAC62I3C8233LACTIB
SUS SCROFA JEJUNUMTA501QD69RACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
SUS SCROFA LUNG7GL3G1COB3ACTIB
SUS SCROFA NASAL MUCOSAID3Z1X61WYACTIB
SODIUM DIETHYL OXALACETATE6CA025Y4FGACTIB
SUS SCROFA ORAL MUCOSADUP6W562BMACTIB
SUS SCROFA PANCREAS9Y3J3362RYACTIB
PHOSPHORUS27YLU75U4WACTIB
SUS SCROFA RECTAL MUCOSA03T60V100YACTIB
SUS SCROFA STOMACHT0920P9Z9AACTIB
SULFUR70FD1KFU70ACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
YEAST MANNAN91R887N59PACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
MANDRAGORA OFFICINARUM ROOTI2XCB174VBACTIB
SUS SCROFA URINARY BLADDER3G7U72W8DAACTIB
SHIGELLA DYSENTERIAE1EP6R5562JACTIB
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
3d745f48-8ca9-4e82-a1e8-6b9bf60380b5e94fbfeb-cf8e-4aff-83e4-5de6bf7e3af72021-12-23WarningsExact identifier
spl id: 3d745f48-8ca9-4e82-a1e8-6b9bf60380b5
spl set id: e94fbfeb-cf8e-4aff-83e4-5de6bf7e3af7

Reported adverse events (FAERS/openFDA)#

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