Label: RUTA GRAVEOLENS- ruta graveolens flowering top liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71919-595-07, 71919-595-08, 71919-595-09, 71919-595-10 - Packager: Washington Homeopathic Products
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 Label Information
Updated December 31, 2009
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- USES
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS
- STOP USE AND ASK DOCTOR
- DIRECTIONS
- INACTIVE INGREDIENTS
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PRINCIPAL DISPLAY PANEL
The OTC potency range of RUTA is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.
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.
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INGREDIENTS AND APPEARANCE
RUTA GRAVEOLENS
ruta graveolens flowering top liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71919-595 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (RUTA GRAVEOLENS FLOWERING TOP - UNII:N94C2U587S) RUTA GRAVEOLENS FLOWERING TOP 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:71919-595-07 15 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/31/2009 2 NDC:71919-595-08 30 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product 12/31/2009 3 NDC:71919-595-09 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/31/2009 4 NDC:71919-595-10 100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 12/31/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/31/2009 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(71919-595)