VISCUM SALIX RK 23X liquid

Viscum Salix RK 23X by

Drug Labeling and Warnings

Viscum Salix RK 23X by is a Homeopathic medication manufactured, distributed, or labeled by True Botanica, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Viscum Album 23X, HPUS

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

PURPOSE

For contitutional treatments based on homeopathic and anthroposophic indications or as directed by your physician.

Use:

For contitutional treatments based on homeopathic and anthroposophic 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. Adults3-5 drops 3 times a day. Children 2-12 years--3-5 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, 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

VISCUM SALIX RK 23X 
viscum salix rk 23x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53645-2161
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
VISCUM ALBUM WHOLE (UNII: E6839Q6DO1) (VISCUM ALBUM WHOLE - UNII:E6839Q6DO1)	VISCUM ALBUM WHOLE	23 [hp_X]  in 20 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53645-2161-4	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/02/2025

Labeler - True Botanica, LLC (182071519)

Establishment
Name	Address	ID/FEI	Business Operations
True Botanica, LLC		182071519	manufacture(53645-2161)