Aurum Metallicum by True Botanica, LLC AURUM METALLICUM liquid

Aurum Metallicum by

Drug Labeling and Warnings

Aurum Metallicum by is a Homeopathic medication manufactured, distributed, or labeled by True Botanica, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Aurum Metallicum 6X, HPUS

The letters HPUS indicate that these ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.

PURPOSE

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Use:

For the temporary relief of weak memory, low mood, heart palpitations, noise sensitivity, poor tissue healing. May also be used for standard homeopathic indications or as directed by your physician.

Warnings:

Consult your health care provider if symptoms persist more than 5 days or worsen.

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

DO NOT USE

TAMPER EVIDENT: Do not use if safety seal is broken before first use.

Directions for Use:

Place drops under tongue for 30 seconds. Adults~20 drops 3 times a day. Children 2-12 years ~ 5-10
drops 3 times a day. Under 2 years, consult your doctor. Use until symptoms are relieved or as directed by your health care provider.

Other Ingredients:

Citric Acid, Potassium Sorbate, Water.

QUESTIONS

Developed and Made by

True Botanica, LLC

1005 Richards Rd., Suite D

Hartland, WI 53029

800-315-8783

www.truebotanica.com

Principal Display Panel

INGREDIENTS AND APPEARANCE

AURUM METALLICUM 
aurum metallicum liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53645-1020
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	6 [hp_X]  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53645-1020-0	50 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		01/21/2013

Labeler - True Botanica, LLC (182071519)

Establishment
Name	Address	ID/FEI	Business Operations
True Botanica, LLC		182071519	manufacture(53645-1020)