LAPPA MAJOR- arctium lappa root 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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DRUG FACTS

ACTIVE INGREDIENTS

LAPPA

USES

To relieve the symptoms of skin eruptions.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

LAPPA   Skin eruptions

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 LAPPA is 2x–30x, 1c–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.

LAPPA MAJOR 
arctium lappa root liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-404
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (ARCTIUM LAPPA ROOT - UNII:597E9BI3Z3) ARCTIUM LAPPA ROOT30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorwhite (white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71919-404-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product02/03/2010
2NDC:71919-404-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product02/03/2010
3NDC:71919-404-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
4NDC:71919-404-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic02/03/2010
Labeler - Washington Homeopathic Products (084929389)
Establishment
NameAddressID/FEIBusiness Operations
Washington Homeopathic Products084929389manufacture(71919-404)

Revised: 12/2018
Document Id: 7e568311-1e9f-9b4b-e053-2991aa0a7b67
Set id: cda55721-6288-432e-b14b-4b63e3fc77ad
Version: 2
Effective Time: 20181231
 
Washington Homeopathic Products