Home NDC 44911-0905 Influenzinum 200C
Product NDC 44911-0905
11-digit product format 449110905
Labeler code 44911
Product ID 44911-0905_7d7554b1-6f99-46b9-9be4-c6054577087f
Type HUMAN OTC DRUG
Nonproprietary name Influenzinum (2025-2026)
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-04-15
Substance INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA A VIRUS A/CROATIA/10136RV/2023 X-425A (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED); INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 ANTIGEN (PROPIOLACTONE INACTIVATED)
Active strength 200; 200; 200 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Influenzinum 200C
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength INFLUENZA A VIRUS A/VICTORIA/4897/2022 IVR-238 (H1N1) ANTIGEN (PROPIOLACTONE INACTIVATED) 200 [hp_C]/mL INFLUENZA A VIRUS A/CROATIA/10136RV/2023 X-425A (H3N2) ANTIGEN (PROPIOLACTONE INACTIVATED) 200 [hp_C]/mL INFLUENZA B VIRUS B/AUSTRIA/1359417/2021 BVR-26 ANTIGEN (PROPIOLACTONE INACTIVATED) 200 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination UPH9LRJ9HU Internal UNII lookup L38QVJ42SY Internal UNII lookup 5UFQ6ZRS6Y Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0905-1 Influenzinum 200C 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
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 Sample Exclude flag Status 44911-0905-1 44911090501 30 mL in 1 BOTTLE, DROPPER (44911-0905-1) 30 ml 2026-04-15 No No Current