G-56- ulmus glabra whole and cedrus libani whole solution
DNA Labs, Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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G-56

NDC 58264-0419-2

INDICATIONS

Irritation, congestion.

INGREDIENTS

ACTIVE

Ulmus campestris (Elm) 1DH, Cedrus libani (Cedar of Lebanon) 1DH

INACTIVE

36.6% alcohol (V/V) Glycerin Macerate

SUGGESTED DOSAGE

One dropper full twice daily.

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.

To be used according to standard homeopathic indications.

PRINCIPAL DISPLAY PANEL - 2 FL. OZ. Bottle Label

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

G-56

DERMAL
DRAINER

GEMMOTHERAPY

2 FL. OZ.

G-56
ulmus glabra whole and cedrus libani whole solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58264-0419
Route of Administration	SUBLINGUAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ULMUS GLABRA WHOLE (UNII: I2AHJ0JD5V) (ULMUS GLABRA WHOLE - UNII:I2AHJ0JD5V)	ULMUS GLABRA WHOLE	1 [hp_X] in 1 mL
CEDRUS LIBANI WHOLE (UNII: 9G0JE54296) (CEDRUS LIBANI WHOLE - UNII:9G0JE54296)	CEDRUS LIBANI WHOLE	1 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:58264-0419-2	59.14 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	01/01/1990

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

Labeler - DNA Labs, Inc. (031784339)