Intercellular Detox

Product NDC
62185-0044
11-digit product format
621850044
Labeler code
62185
Product ID
62185-0044_3d745f48-8ca9-4e82-a1e8-6b9bf60380b5
Type
HUMAN OTC DRUG
Nonproprietary name
Ceanothus Americanus, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (Vulgaris), 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, Mannan,
Dosage form
LIQUID
Route
ORAL
Labeler
Dr. Donna Restivo DC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-03-15
Marketing end
2024-03-15
Substance
CEANOTHUS 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
Active strength
4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62185-0044-12021-12-23C16284748780-1ba0f9c33-25bd-a910-e053-dadaa90a0b85e94fbfeb-cf8e-4aff-83e4-5de6bf7e3af7
62185-0044-12021-01-29C16284748780-1ba0f9c33-25bd-a910-e053-dadaa90a0b85e94fbfeb-cf8e-4aff-83e4-5de6bf7e3af7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62185-0044-16218500440130 mL in 1 BOTTLE, DROPPER (62185-0044-1) 30 ml2019-03-152024-03-15NoNoCurrent