COCCULUS INDICUS- anamirta cocculus seed 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.

----------

DRUG FACTS

ACTIVE INGREDIENTS

COCCULUS

USES

To relieve the symptoms of motion sickness.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

COCCULUS   Motion sickness

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 COCCULUS is 4x–30x, 2c–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.

COCCULUS INDICUS 
anamirta cocculus seed liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-212
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U) ANAMIRTA COCCULUS SEED 30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color white (white) Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:71919-212-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/03/2010
2 NDC:71919-212-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 02/03/2010
3 NDC:71919-212-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/03/2010
4 NDC:71919-212-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/03/2010
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 02/03/2010
Labeler - Washington Homeopathic Products (084929389)
Establishment
Name Address ID/FEI Business Operations
Washington Homeopathic Products 084929389 manufacture(71919-212)

Revised: 12/2018
Document Id: 7e46dafe-d806-3cea-e053-2a91aa0aaae5
Set id: f9097ada-1bdd-4d91-b2d7-61e71ac83c24
Version: 2
Effective Time: 20181230
 
Washington Homeopathic Products