KALI CYANATUM- potassium cyanide liquid
Washington Homeopathic Products

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Kali cyanatum X

ACTIVE INGREDIENTS

KALI CYAN

USES

To relieve the symptoms of tongue ulcers.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications:

KALI CYAN Tongue ulcers

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.

DIRECTIONS

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

The OTC potency range of KALI CYAN is 8x–30x, 4c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Label

All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled.

‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice.

Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml.

KALI CYANATUM
potassium cyanide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71919-382
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POTASSIUM CYANIDE (UNII: MQD255M2ZO) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CYANIDE	30 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white (white)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71919-382-07	15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	07/25/2015
2	NDC:71919-382-08	30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product	07/25/2015
3	NDC:71919-382-09	50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	07/25/2015
4	NDC:71919-382-10	100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	07/25/2015

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/25/2015	03/23/2022

Labeler - Washington Homeopathic Products (084929389)

Name	Address	ID/FEI	Business Operations
Establishment
Washington Homeopathic Products		084929389	manufacture(71919-382)

Revised: 3/2022

Document Id: dae5c0f7-4a1b-2ae7-e053-2995a90a5675

Set id: 450c531b-0758-4c82-b6ed-83c8bf010dc2

Version: 3

Effective Time: 20220323

Washington Homeopathic Products