Fungustat

Product NDC
44911-0497
11-digit product format
449110497
Labeler code
44911
Product ID
44911-0497_00dff638-e674-46a1-9bff-55b422f30e97
Type
HUMAN OTC DRUG
Nonproprietary name
Echinacea (Angustifolia), Tabebuia Impetiginosa, Abies Nigra, Lycopodium Clavatum, Nux Vomica, Phosphorus, Pulsatilla (Pratensis), Sepia, Skatolum, Candida Albicans
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-05-15
Marketing end
2024-07-23
Substance
CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA WHOLE; HANDROANTHUS IMPETIGINOSUS BARK; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; PICEA MARIANA RESIN; PULSATILLA PRATENSIS WHOLE; SEPIA OFFICINALIS JUICE; SKATOLE; STRYCHNOS NUX-VOMICA SEED
Active strength
30 [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
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
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
44911-0497-12022-03-09C16284748780-1ba0f9c33-3b67-a910-e053-dadaa90a0b851ec4b1e4-7e5d-4c8e-975e-25708a121f25
44911-0497-12021-01-29C16284748780-1ba0f9c33-3b67-a910-e053-dadaa90a0b851ec4b1e4-7e5d-4c8e-975e-25708a121f25

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0497-14491104970160 mL in 1 BOTTLE, DROPPER (44911-0497-1) 60 ml2019-05-152024-07-23NoNoCurrent