G-56

Product NDC: 58264-0419
Requested package NDC: 58264-0419-2
11-digit product format: 582640419
Labeler code: 58264
Product ID: 58264-0419_2b53486e-1970-6db9-e063-6294a90a24ab
Type: HUMAN OTC DRUG
Nonproprietary name: ulmus glabra whole and cedrus libani whole
Dosage form: SOLUTION
Route: SUBLINGUAL
Labeler: DNA Labs, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 1990-01-01
Substance: ULMUS GLABRA WHOLE; CEDRUS LIBANI WHOLE
Active strength: 1; 1 [hp_X]/mL; [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…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: G-56
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ULMUS GLABRA WHOLE	1 [hp_X]/mL
CEDRUS LIBANI WHOLE	1 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
I2AHJ0JD5V	Internal UNII lookup
9G0JE54296	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
62aa0420-2bbd-4b1b-9c94-d971739f4b8e	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0419-2	2022-06-08	C162847	48780-1	9d75b9d0-374e-f424-e053-dadaa90a57ce	G-56
58264-0419-2	2020-01-31	C162847	48780-1	9d75b9d0-374e-f424-e053-dadaa90a57ce	G-56

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0419-2	G-56	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
58264-0419	G-56 (ULMUS GLABRA WHOLE AND CEDRUS LIBANI WHOLE) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250112_62aa0420-2bbd-4b1b-9c94-d971739f4b8e.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-56	ULMUS GLABRA WHOLE AND CEDRUS LIBANI WHOLE	DNA Labs, Inc.	62aa0420-2bbd-4b1b-9c94-d971739f4b8e	2025-01-09	Warnings	Exact identifier ndc (package): 58264-0419-2 ndc (product): 58264-0419 ndc11 (package): 58264041902

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
I2AHJ0JD5V	ULMUS GLABRA WHOLE	ULMUS GLABRA WHOLE
9G0JE54296	CEDRUS LIBANI WHOLE	CEDRUS LIBANI WHOLE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
58264-0419-2	58264041902	59.14 mL in 1 BOTTLE, GLASS (58264-0419-2)	59.14 ml	1990-01-01	0000-00-00	No	No	Current