ARTEMISIA VULGARIS- artemisia vulgaris root pellet 
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

ARTEMISIA   30C

USES

To relieve the symptoms of fainting.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications:

ARTEMISIA   Dizziness

STOP USE AND ASK DOCTOR

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

DIRECTIONS

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

The OTC potency range of ARTEMISIA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.

Artemisia label example

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’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

ARTEMISIA VULGARIS 
artemisia vulgaris root pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68428-892
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (ARTEMISIA VULGARIS ROOT - UNII:32MP823R8S) ARTEMISIA VULGARIS ROOT30 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Product Characteristics
Colorwhite (white) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68428-892-0375 in 1 VIAL, GLASS; Type 0: Not a Combination Product04/06/2011
2NDC:68428-892-05150 in 1 VIAL, GLASS; Type 0: Not a Combination Product04/06/2011
3NDC:68428-892-11300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/06/2011
4NDC:68428-892-12600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/06/2011
5NDC:68428-892-061200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/06/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic04/06/2011
Labeler - Washington Homeopathic Products (084929389)
Establishment
NameAddressID/FEIBusiness Operations
Washington Homeopathic Products084929389manufacture(68428-892)

Revised: 11/2016
Document Id: f43dbeb7-abff-4363-8112-f178af218cb2
Set id: b677f6c8-c2fa-4834-a71c-698cd2660af0
Version: 1
Effective Time: 20161128
 
Washington Homeopathic Products