G-41

Manufacturer: DNA Labs, Inc.
Effective date: 2025-01-09
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:30:56

Label at a glance#

ProductG-41

Active ingredientULMUS GLABRA WHOLE

Label structure9 sections

Storage and handling

SHAKE WELL

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

NDC 58264-0404-2

INDICATIONS

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Support for the joints and skin.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ACTIVE

SPL UNCLASSIFIED SECTION

Ulmus campestris (Elm) 1DH

INACTIVE

INACTIVE INGREDIENT SECTION

36.6% alcohol (V/V) Glycerin Macerate

Rx CAUTION

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without a prescription.

SUGGESTED DOSAGE

DOSAGE & ADMINISTRATION SECTION

One dropper full twice daily.

STORAGE AND HANDLING SECTION

SHAKE WELL

Warnings

WARNINGS SECTION

Use only if cap seal is unbroken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medication out of the reach of children.

SPL UNCLASSIFIED SECTION

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

G-41

ULMUS
CAMPESTRIS

GEMMOTHERAPY

2 FL. OZ.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58264-0404-2	2022-06-08	C162847	48780-1	9d75b9d1-1326-f424-e053-dadaa90a57ce	G-41
58264-0404-2	2020-01-31	C162847	48780-1	9d75b9d1-1326-f424-e053-dadaa90a57ce	G-41

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58264-0404-2	G-41	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
58264-0404	G-41 (ULMUS GLABRA WHOLE) SOLUTION [DNA LABS, INC.]	3	Current NDC, Legacy NDC, 1 package rows	20250112_9dc69a72-b1ac-4401-8c38-ccc9d775fdfc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

G-41
ULMUS GLABRA WHOLE
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58264-0404	58264-0404-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
ULMUS GLABRA WHOLE	I2AHJ0JD5V	ACTIB

Source Document#

Source XML

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-41	ULMUS GLABRA WHOLE	DNA Labs, Inc.	9dc69a72-b1ac-4401-8c38-ccc9d775fdfc	2025-01-09	Warnings	Exact identifier ndc (package): 58264-0404-2 ndc (product): 58264-0404 ndc11 (package): 58264040402 spl id: 2b533c4d-d42d-4cac-e063-6294a90a7d51 spl set id: 9dc69a72-b1ac-4401-8c38-ccc9d775fdfc

Reported adverse events (FAERS/openFDA)#

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