D17- naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide solution

D17 by

Drug Labeling and Warnings

D17 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: 58264-0017-1

INDICATIONS

Regenerator of diseased tissue.

ACTIVE INGREDIENT

INGREDIENTS

Scrophularia nodosa 2x, Acidum lactium 4x, Radium bromatum 30x, Naja tripudians 30x, 24% alcohol in purified water.

RX CAUTION

Federal law prohibits dispensing without a prescription.

SUGGESTED DOSAGE

One dropper full under the tongue two times daily. In acute conditions 5-10 drops under the tongue every 20-30 minutes.

STORAGE AND HANDLING

SHAKE WELL

Warnings

• Use only if cap seal is unbroken.

• As with drugs if you are pregnant or nursing a baby seek professional advice before using this product.

• 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 17

HOMEOPATHIC FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D17 
naja naja whole, scrophularia nodosa, lactic acid, dl-, and radium bromide solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0017
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Naja Naja Whole (UNII: D279BDR31E) (Naja Naja Whole - UNII:D279BDR31E)	Naja Naja Whole	30 [hp_X]  in 1 mL
Scrophularia nodosa (UNII: 7H443NUB2T) (Scrophularia nodosa - UNII:7H443NUB2T)	Scrophularia nodosa	2 [hp_X]  in 1 mL
Lactic Acid, DL- (UNII: 3B8D35Y7S4) (Lactic Acid, DL- - UNII:3B8D35Y7S4)	Lactic Acid, DL-	4 [hp_X]  in 1 mL
Radium bromide (UNII: R74O7T8569) (Radium Cation - UNII:05456MVL7T)	Radium bromide	30 [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: 58264-0017-1	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)