D-10- sepia officinalis whole, sanguinaria canadensis root, sulfuric acid, black cohosh, and lachesis muta venom solution

D-10 by

Drug Labeling and Warnings

D-10 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: 58264-0010-1

INDICATIONS

Flushes of heat.

INGREDIENTS

ACTIVE

Sepia officinalis 4x, Sanguinaria canadensis 4x, Acidum sulfuricum 4x, Cimicifuga 4x, Lachesis mutus 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 10

HOMEOPATHIC
STRESS FORMULA

1 FL. OZ.

INGREDIENTS AND APPEARANCE

D-10 
sepia officinalis whole, sanguinaria canadensis root, sulfuric acid, black cohosh, and lachesis muta venom solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58264-0010
Route of Administration	SUBLINGUAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sepia officinalis whole (UNII: 48GD5780QF) (Sepia officinalis whole - UNII:48GD5780QF)	Sepia officinalis whole	4 [hp_X]  in 1 mL
Sanguinaria canadensis root (UNII: N9288CD508) (Sanguinaria canadensis root - UNII:N9288CD508)	Sanguinaria canadensis root	4 [hp_X]  in 1 mL
Sulfuric acid (UNII: O40UQP6WCF) (Sulfuric acid - UNII:O40UQP6WCF)	Sulfuric acid	4 [hp_X]  in 1 mL
Black cohosh (UNII: K73E24S6X9) (Black cohosh - UNII:K73E24S6X9)	Black cohosh	4 [hp_X]  in 1 mL
Lachesis muta venom (UNII: VSW71SS07I) (Lachesis muta venom - UNII:VSW71SS07I)	Lachesis muta venom	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: 58264-0010-1	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)