D-51- atropa belladonna, iodine, lycopus virginicus, sodium chloride, hekla lava, and calcium hexafluorosilicate solution

D-51 by

Drug Labeling and Warnings

D-51 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: 58264-0051-1

INDICATIONS

Thyroid health.

INGREDIENTS

ACTIVE

Belladonna 30x, Iodium 30x, Lycopus virginicus 12x, Natrum muriaticum 30x, Hekla lava 12x, Lapis albus 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 51

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D-51 
atropa belladonna, iodine, lycopus virginicus, sodium chloride, hekla lava, and calcium hexafluorosilicate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0051
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Atropa belladonna (UNII: WQZ3G9PF0H) (Atropa belladonna - UNII:WQZ3G9PF0H)	Atropa belladonna	30 [hp_X]  in 1 mL
Iodine (UNII: 9679TC07X4) (Iodine - UNII:9679TC07X4)	Iodine	30 [hp_X]  in 1 mL
Lycopus virginicus (UNII: TWH5125Q6F) (Lycopus virginicus - UNII:TWH5125Q6F)	Lycopus virginicus	12 [hp_X]  in 1 mL
Sodium chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37)	Sodium chloride	30 [hp_X]  in 1 mL
Hekla lava (UNII: C21158IIRK) (Hekla lava - UNII:C21158IIRK)	Hekla lava	12 [hp_X]  in 1 mL
Calcium Hexafluorosilicate (UNII: 2NVP93XVQ3) (Calcium Hexafluorosilicate - UNII:2NVP93XVQ3)	Calcium Hexafluorosilicate	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: 58264-0051-1	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)