Home NDC 44911-0190 Glutathione
Product NDC 44911-0190
11-digit product format 449110190
Labeler code 44911
Product ID 44911-0190_7c8fa016-41f0-41e4-8b1c-1533e6d7aa36
Type HUMAN OTC DRUG
Nonproprietary name Glutathione
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-07-09
Substance GLUTATHIONE
Active strength 5 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Glutathione
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GLUTATHIONE 5 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination GAN16C9B8O 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 44911-0190-1 Glutathione 30 mL in 1 BOTTLE, DROPPER LIQUID 30 3
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
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
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 44911-0190-1 44911019001 30 mL in 1 BOTTLE, DROPPER (44911-0190-1) 30 ml 2015-07-09 0000-00-00 No No Current