G-4

Product NDC: 58264-0367
Requested package NDC: 58264-0367-2
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

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 5 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	`9bebd1f3094a…`	`5416666fcb17…`

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 UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
83F04L6KZ4	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2ebaaa87-0fd0-4f48-b9c1-6d0c93b44d65	Available on FDA.report

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

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
G-4	ALNUS GLUTINOSA LEAF	DNA Labs, Inc.	2ebaaa87-0fd0-4f48-b9c1-6d0c93b44d65	2025-01-09	Warnings	Exact identifier ndc (package): 58264-0367-2 ndc (product): 58264-0367 ndc11 (package): 58264036702

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
83F04L6KZ4	ALNUS GLUTINOSA LEAF	ALNUS GLUTINOSA LEAF

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

G-4