D-33- atropa belladonna, bufo bufo cutaneous gland, copper, anemone pratensis, silicon dioxide, and zinc solution

D-33 by

Drug Labeling and Warnings

D-33 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: 58264-0033-1

INDICATIONS

Epilepsy, irritations of the nerve.

INGREDIENTS

ACTIVE

Belladonna 30x, Bufo rana 200x, Cuprum metallicum 12x, Pulsatilla 30x, Silicea 30x, Zincum metallicum 12x

INACTIVE

20% alcohol in purified water.

Rx CAUTION

Federal law prohibits dispensing without a 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 33

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D-33 
atropa belladonna, bufo bufo cutaneous gland, copper, anemone pratensis, silicon dioxide, and zinc solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0033
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
BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (BUFO BUFO CUTANEOUS GLAND - UNII:Q59QU6N72Q)	BUFO BUFO CUTANEOUS GLAND	200 [hp_X]  in 1 mL
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	12 [hp_X]  in 1 mL
ANEMONE PRATENSIS (UNII: 8E272251DI) (ANEMONE PRATENSIS - UNII:8E272251DI)	ANEMONE PRATENSIS	30 [hp_X]  in 1 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	30 [hp_X]  in 1 mL
ZINC (UNII: J41CSQ7QDS) (ZINC - UNII:J41CSQ7QDS)	ZINC	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: 58264-0033-1	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)