Home NDC 44911-0190-01 NDC 44911-0190-01 - Glutathione This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 44911-0190
Requested NDC 44911-0190-01
Package NDCs from labels 44911-0190-1, 44911-0190-01
Manufacturer Energique, Inc. | Apotheca Company
Effective date 2026-09-02
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0190-1 Glutathione 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 44911-0190 GLUTATHIONE LIQUID [ENERGIQUE, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20230223_3a369e12-984c-4b94-9b77-eb8d77c545bb.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded GLUTATHIONE ACTIVE INGREDIENT GAN16C9B8O GLUTATHIONE (GLUTATHIONE,) LIQUID [ENERGIQUE, INC.] 1 GLUTATHIONE ACTIVE MOIETY GAN16C9B8O GLUTATHIONE (GLUTATHIONE,) LIQUID [ENERGIQUE, INC.] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M GLUTATHIONE (GLUTATHIONE,) LIQUID [ENERGIQUE, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R GLUTATHIONE (GLUTATHIONE,) LIQUID [ENERGIQUE, INC.] 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 12 of 149 · 2,967 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.