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: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
GLUTATHIONE	5 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	GAN16C9B8O

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

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