Oligo Bio Iodine

Product NDC
43857-0515
11-digit product format
438570515
Labeler code
43857
Product ID
43857-0515_a9f86fd3-836d-409e-ab02-ae16b42c9d55
Type
HUMAN OTC DRUG
Nonproprietary name
Chelidonium Majus, Spongia Tosta, Iodium, Lycopus Virginicus, Ginkgo Biloba, Pinus Sylvestris, Fucus Vesiculosus, Germanium Sesquioxide, Hypophysis Suis, Thyroidinum (Suis), Cysteinum, Manganese Gluconate, alpha-Ketoglutaricum Acidum, Calcarea Carbonica, Ferrum Iodatum, Fumaricum Acidum, Kali Iodatum, Natrum Oxalaceticum, Pulsatilla (Vulgaris), Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum,
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-06-27
Marketing end
2024-11-06
Substance
CHELIDONIUM MAJUS; SPONGIA OFFICINALIS SKELETON, ROASTED; IODINE; LYCOPUS VIRGINICUS; GINKGO; PINUS SYLVESTRIS LEAFY TWIG; FUCUS VESICULOSUS; GERMANIUM SESQUIOXIDE; SUS SCROFA PITUITARY GLAND; SUS SCROFA THYROID; CYSTEINE; MANGANESE GLUCONATE; OXOGLURIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FERROUS IODIDE; FUMARIC ACID; POTASSIUM IODIDE; SODIUM DIETHYL OXALACETATE; ANEMONE PULSATILLA; SILVER; GOLD; COPPER; EUGENOL; FORMALDEHYDE; LIDOCAINE; MERCURIUS SOLUBILIS; MOLYBDENUM; NICKEL; PALLADIUM; TIN; TITANIUM; ZINC; RUBELLA VIRUS; MUMPS VIRUS; HUMAN COXSACKIEVIRUS A2; HUMAN COXSACKIEVIRUS A7; HUMAN COXSACKIEVIRUS B1; HUMAN COXSACKIEVIRUS B3; HUMAN COXSACKIEVIRUS B4
Active strength
3 [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_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/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
43857-0515-12021-06-16C16284748780-1ba0f9c33-1311-a910-e053-dadaa90a0b8503dfd9c7-d0d5-4fa4-8d7d-4e39d9373d59
43857-0515-12021-01-29C16284748780-1ba0f9c33-1311-a910-e053-dadaa90a0b8503dfd9c7-d0d5-4fa4-8d7d-4e39d9373d59

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43857-0515-14385705150160 mL in 1 BOTTLE, DROPPER (43857-0515-1) 60 ml2019-06-272024-11-06NoNoCurrent