D-39- lachesis muta venom, lycopodium clavatum spore, palladium, saxifraga granulata whole, and vespa crabro solution

D-39 by

Drug Labeling and Warnings

D-39 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: 58264-0039-1

INDICATIONS

Supports ovary on the left side.

INGREDIENTS

ACTIVE

Lachesis mutus 30x, Lycopodium clavatum 30x, Palladium metallicum 12x, Saxifraga granulata 30x, Vespa crabro 12x

INACTIVE

20% alcohol in purified water.

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 39

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D-39 
lachesis muta venom, lycopodium clavatum spore, palladium, saxifraga granulata whole, and vespa crabro solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0039
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	30 [hp_X]  in 1 mL
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	30 [hp_X]  in 1 mL
PALLADIUM (UNII: 5TWQ1V240M) (PALLADIUM - UNII:5TWQ1V240M)	PALLADIUM	12 [hp_X]  in 1 mL
SAXIFRAGA GRANULATA WHOLE (UNII: W1LUS9R48G) (SAXIFRAGA GRANULATA WHOLE - UNII:W1LUS9R48G)	SAXIFRAGA GRANULATA WHOLE	30 [hp_X]  in 1 mL
Vespa crabro (UNII: K3ALM8S49H) (Vespa crabro - UNII:K3ALM8S49H)	Vespa crabro	12 [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: 58264-0039-1	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)