Intercellular Detox

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Intercellular Detox
Generic name: CEANOTHUS AMERICANUS, ARGENTUM NITRICUM, CONDURANGO, HYDRASTIS CANADENSIS, MOMORDICA BALSAMINA, PULSATILLA (PRATENSIS), BILE DUCT (SUIS), COLON (SUIS), DUODENUM (SUIS), ESOPHAGUS (SUIS), EYE (SUIS), GALLBLADDER (SUIS), ILEUM (SUIS), INTESTINE (SUIS), IPECACUANHA, JEJUNUM (SUIS), KALI BICHROMICUM, LUNG (SUIS), MUCOSA NASALIS SUIS, NATRUM OXALACETICUM, ORAL MUCOSA (SUIS), PANCREAS SUIS, PHOSPHORUS, RECTAL MUCOSA (SUIS), STOMACH (SUIS), SULPHUR, VERATRUM ALBUM, MANNOSE, ANACARDIUM ORIENTALE, KREOSOTUM,
Manufacturer: Dr. Donna Restivo DC
Product type: HUMAN OTC DRUG
SPL set ID: 981bc6f9-05da-40cf-9ba0-37acc524f9f8
SPL ID: 79a3f971-033d-4add-a537-9a397d561634
Version: 3
Effective date: 2024-01-18
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:59

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 2 · 42 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Intercellular Detox	openfda.brand_name
generic name		CEANOTHUS AMERICANUS, ARGENTUM NITRICUM, CONDURANGO, HYDRASTIS CANADENSIS, MOMORDICA BALSAMINA, PULSATILLA (PRATENSIS), BILE DUCT (SUIS), COLON (SUIS), DUODENUM (SUIS), ESOPHAGUS (SUIS), EYE (SUIS), GALLBLADDER (SUIS), ILEUM (SUIS), INTESTINE (SUIS), IPECACUANHA, JEJUNUM (SUIS), KALI BICHROMICUM, LUNG (SUIS), MUCOSA NASALIS SUIS, NATRUM OXALACETICUM, ORAL MUCOSA (SUIS), PANCREAS SUIS, PHOSPHORUS, RECTAL MUCOSA (SUIS), STOMACH (SUIS), SULPHUR, VERATRUM ALBUM, MANNOSE, ANACARDIUM ORIENTALE, KREOSOTUM,	openfda.generic_name
manufacturer name		Dr. Donna Restivo DC	openfda.manufacturer_name
ndc	package	62185-0055-1	openfda.package_ndc
ndc	product	62185-0055	openfda.product_ndc
ndc11	package	62185005501	derived:openfda.package_ndc
spl id		79a3f971-033d-4add-a537-9a397d561634	id
spl set id		981bc6f9-05da-40cf-9ba0-37acc524f9f8	set_id
unii		27YLU75U4W	openfda.unii
unii		T0920P9Z9A	openfda.unii
unii		U1W3U02EW0	openfda.unii
unii		7GL3G1COB3	openfda.unii
unii		I2XCB174VB	openfda.unii
unii		1EP6R5562J	openfda.unii
unii		94J255A0UC	openfda.unii
unii		81FZ7X4MWD	openfda.unii
unii		4EE983392U	openfda.unii
unii		ID3Z1X61WY	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		DUP6W562BM	openfda.unii
unii		X3AOK514E6	openfda.unii
unii		TA501QD69R	openfda.unii
unii		3G7U72W8DA	openfda.unii
unii		P6J2SFT80O	openfda.unii
unii		25B1Y14T8N	openfda.unii
unii		8E272251DI	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		62I3C8233L	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		C998R1XSRA	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		T4423S18FM	openfda.unii
unii		B6A98VOI9I	openfda.unii
unii		3JYG22FD73	openfda.unii
unii		Y0F0BU8RDU	openfda.unii
unii		6CA025Y4FG	openfda.unii
unii		WUW1665V10	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		03T60V100Y	openfda.unii
unii		40GMI0R60L	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: 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.

Reported adverse events (FAERS/openFDA)#

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