G-41- ulmus glabra whole solution

G-41 by

Drug Labeling and Warnings

G-41 by is a Homeopathic medication manufactured, distributed, or labeled by DNA Labs, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

NDC: 58264-0404-2

INDICATIONS

Support for the joints and skin.

INGREDIENTS

ACTIVE

Ulmus campestris (Elm) 1DH

INACTIVE

36.6% alcohol (V/V) Glycerin Macerate

Rx CAUTION

Federal law prohibits dispensing without a prescription.

SUGGESTED DOSAGE

One dropper full twice daily.

STORAGE AND HANDLING

SHAKE WELL

Warnings

• Use only if cap seal is unbroken.

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

• 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

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

G-41

ULMUS
CAMPESTRIS

GEMMOTHERAPY

2 FL. OZ.

INGREDIENTS AND APPEARANCE

G-41 
ulmus glabra whole solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0404
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ULMUS GLABRA WHOLE (UNII: I2AHJ0JD5V) (ULMUS GLABRA WHOLE - UNII:I2AHJ0JD5V)	ULMUS GLABRA WHOLE	1 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Alcohol (UNII: 3K9958V90M)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58264-0404-2	59.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/1990

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved homeopathic		01/01/1990

Labeler - DNA Labs, Inc. (031784339)