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

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.

SHAKE WELL

Warnings

  • 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 59

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
D-59 
fucus vesiculosus, spongia officinalis skeleton, roasted, graphite, oyster shell calcium carbonate, crude, sodium sulfate, and croton oil solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58264-0059
Route of AdministrationSUBLINGUAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS3 [hp_X]  in 1 mL
SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED3 [hp_X]  in 1 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE12 [hp_X]  in 1 mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE12 [hp_X]  in 1 mL
SODIUM SULFATE (UNII: 0YPR65R21J) (SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750) SODIUM SULFATE2 [hp_X]  in 1 mL
CROTON OIL (UNII: WK97EQG57S) (CROTON OIL - UNII:WK97EQG57S) CROTON OIL4 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58264-0059-129.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/01/1990
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/01/1990
Labeler - DNA Labs, Inc. (031784339)

Revised: 6/2022
Document Id: e0836408-fe09-748e-e053-2995a90a79b0
Set id: b153cf23-eb3b-4647-b7f4-44380d498334
Version: 2
Effective Time: 20220602
 
DNA Labs, Inc.