Home NDC 44911-0544 Candida Combo
Product NDC 44911-0544
11-digit product format 449110544
Labeler code 44911
Product ID 44911-0544_d4900e0d-4def-4030-af22-30b4355dbe55
Type HUMAN OTC DRUG
Nonproprietary name Candida Albicans, Candida Krusei, Candida Parapsilosis
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-04-30
Substance CANDIDA ALBICANS; ISSATCHENKIA ORIENTALIS WHOLE; CANDIDA PARAPSILOSIS
Active strength 15; 15; 15 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Candida Combo
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CANDIDA ALBICANS 15 [hp_C]/mL ISSATCHENKIA ORIENTALIS WHOLE 15 [hp_C]/mL CANDIDA PARAPSILOSIS 15 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4D7G21HDBC Internal UNII lookup 138TJ2U1SD Internal UNII lookup 0KZ676D44N Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0544-1 Candida Combo 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0544 CANDIDA COMBO (CANDIDA ALBICANS, CANDIDA KRUSEI, CANDIDA PARAPSILOSIS) LIQUID [ENERGIQUE, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20240124_9a794fb7-db06-43bf-835c-b1807b3f9be0.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0544-1 44911054401 30 mL in 1 BOTTLE, DROPPER (44911-0544-1) 30 ml 2020-04-30 0000-00-00 No No Current