G-4

Product NDC: 58264-0367
11-digit product format: 582640367
Labeler code: 58264
Product ID: 58264-0367_2b533cf6-06e7-54d1-e063-6394a90a125b
Type: HUMAN OTC DRUG
Nonproprietary name: Alnus glutinosa leaf
Dosage form: SOLUTION
Route: SUBLINGUAL
Labeler: DNA Labs, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1990-01-01
Substance: ALNUS GLUTINOSA LEAF
Active strength: 1 [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: G-4
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALNUS GLUTINOSA LEAF	1 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	83F04L6KZ4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0367-2	2022-06-08	C162847	48780-1	9d75b9d0-8f92-f424-e053-dadaa90a57ce	G-4
58264-0367-2	2020-01-31	C162847	48780-1	9d75b9d0-8f92-f424-e053-dadaa90a57ce	G-4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0367-2	G-4	59.14 mL in 1 BOTTLE, GLASS	SOLUTION	59.14		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58264-0367	G-4 (ALNUS GLUTINOSA LEAF) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250112_2ebaaa87-0fd0-4f48-b9c1-6d0c93b44d65.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
58264-0367-2	58264036702	59.14 mL in 1 BOTTLE, GLASS (58264-0367-2)	59.14 ml	1990-01-01	0000-00-00	No	No	Current