Label: HENDEL RHUS TOX- toxicodendron pubescens leaf tablet
- NDC Code(s): 62795-1127-2
- Packager: MediNatura Inc
- 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 August 22, 2022
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WARNINGS
If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Rhus Tox 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.
- USES
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- INDICATIONS
- INACTIVE INGREDIENT
- INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HENDEL RHUS TOX
toxicodendron pubescens leaf tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1127 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 6 [hp_X] Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code LEAFMAN Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62795-1127-2 100 in 1 BOTTLE; Type 0: Not a Combination Product 07/12/2016 01/31/2027 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/12/2016 01/31/2027 Labeler - MediNatura Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura Inc 102783016 manufacture(62795-1127)