D-59- fucus vesiculosus, spongia officinalis skeleton, roasted, graphite, oyster shell calcium carbonate, crude, sodium sulfate, and croton oil solution

D-59 by

Drug Labeling and Warnings

D-59 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: 58264-0059-1

INDICATIONS

Tendency to put on weight, slimming effect.

INGREDIENTS

ACTIVE

Fucus vesiculosus 3x, Spongia tosta 3x, Graphites 12x, Calcarea carbonica 12x, Natrum sulfuricum 2x, Croton tiglium 4x

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 59

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D-59 
fucus vesiculosus, spongia officinalis skeleton, roasted, graphite, oyster shell calcium carbonate, crude, sodium sulfate, and croton oil solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0059
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Fucus vesiculosus (UNII: 535G2ABX9M) (Fucus vesiculosus - UNII:535G2ABX9M)	Fucus vesiculosus	3 [hp_X]  in 1 mL
Spongia officinalis skeleton, roasted (UNII: 1PIP394IID) (Spongia officinalis skeleton, roasted - UNII:1PIP394IID)	Spongia officinalis skeleton, roasted	3 [hp_X]  in 1 mL
Graphite (UNII: 4QQN74LH4O) (Graphite - UNII:4QQN74LH4O)	Graphite	12 [hp_X]  in 1 mL
Oyster shell calcium carbonate, crude (UNII: 2E32821G6I) (Oyster shell calcium carbonate, crude - UNII:2E32821G6I)	Oyster shell calcium carbonate, crude	12 [hp_X]  in 1 mL
Sodium sulfate (UNII: 0YPR65R21J) (Sodium sulfate anhydrous - UNII:36KCS0R750)	Sodium sulfate	2 [hp_X]  in 1 mL
Croton oil (UNII: WK97EQG57S) (Croton oil - UNII:WK97EQG57S)	Croton oil	4 [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: 58264-0059-1	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)