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

D-44 by

Drug Labeling and Warnings

D-44 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: 58264-0044-1

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.

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 - 1 FL. OZ. Bottle Label

DYNAMIC
NUTRITIONAL
ASSOCIATES, INC.

D 44

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58264-0044-1	29.57 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)