Label: THUJA OCCIDENTALIS KIT REFILL- thuja occidentalis leafy twig pellet
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Contains inactivated NDC Code(s)
NDC Code(s): 68428-075-01 - 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 13, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- USES
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS
- STOP USE AND ASK DOCTOR
- DIRECTIONS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THUJA OCCIDENTALIS KIT REFILL
thuja occidentalis leafy twig pelletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68428-075 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 200 [hp_C] Inactive Ingredients Ingredient Name Strength SUCROSE (UNII: C151H8M554) LACTOSE (UNII: J2B2A4N98G) 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:68428-075-01 750 in 1 VIAL, GLASS; Type 0: Not a Combination Product 05/03/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/03/2010 Labeler - Washington Homeopathic Products (084929389) Establishment Name Address ID/FEI Business Operations Washington Homeopathic Products 084929389 manufacture(68428-075)