RUBIA TINCTORUM- rubia tinctorum 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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Rubia tinctorum X

ACTIVE INGREDIENTS

RUBIA

USES

To relieve the symptoms of paleness.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications: 

RUBIA   Paleness

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 RUBIA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.
Label
Availability is subject to change.

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.

RUBIA TINCTORUM 
rubia tinctorum root liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71919-591
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G) (RUBIA TINCTORUM ROOT - UNII:0SVP95L23G) RUBIA TINCTORUM 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:71919-591-0715 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product01/14/2009
2NDC:71919-591-0830 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product01/14/2009
3NDC:71919-591-0950 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/14/2009
4NDC:71919-591-10100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product01/14/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/14/200903/24/2022
Labeler - Washington Homeopathic Products (084929389)
Establishment
NameAddressID/FEIBusiness Operations
Washington Homeopathic Products084929389manufacture(71919-591)

Revised: 3/2022
Document Id: daf98334-f95a-5fc3-e053-2a95a90ade60
Set id: defaf163-89e1-43b8-a460-3a4e006cb2d0
Version: 4
Effective Time: 20220324
 
Washington Homeopathic Products