D-44- crataegus laevigata fruit, prunus laurocerasus leaf, nerium oleander leaf, and cytisus scoparius 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.

----------

D-44

NDC 58264-0044-1

INDICATIONS

Circulatory disorders, low blood pressure.

INGREDIENTS

ACTIVE

Crataegus oxyacantha 1x, Laurocerasus 3x, Oleander 6x, Spartium scoparium 6x

INACTIVE

20% alcohol in purified water.

Rx CAUTION

Federal law prohibits dispensing without prescription.

SUGGESTED DOSAGE

One dropper under tongue two times daily. Acute symptoms ½ dropper under tongue every 30 minutes for two hours.

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 - 1 FL. OZ. Bottle Label

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

D 44

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

D-44
crataegus laevigata fruit, prunus laurocerasus leaf, nerium oleander leaf, and cytisus scoparius whole solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:58264-0044
Route of Administration	SUBLINGUAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CRATAEGUS LAEVIGATA FRUIT (UNII: D5RZ7MF1YF) (CRATAEGUS LAEVIGATA FRUIT - UNII:D5RZ7MF1YF)	CRATAEGUS LAEVIGATA FRUIT	1 [hp_X] in 1 mL
PRUNUS LAUROCERASUS LEAF (UNII: F26P2D4757) (PRUNUS LAUROCERASUS LEAF - UNII:F26P2D4757)	PRUNUS LAUROCERASUS LEAF	3 [hp_X] in 1 mL
NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (NERIUM OLEANDER LEAF - UNII:7KV510R6H6)	NERIUM OLEANDER LEAF	6 [hp_X] in 1 mL
CYTISUS SCOPARIUS WHOLE (UNII: V99S891QU7) (CYTISUS SCOPARIUS WHOLE - UNII:V99S891QU7)	CYTISUS SCOPARIUS WHOLE	6 [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:58264-0044-1	29.57 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)