Label: BHI ARTHRITIS- arnica montana root, berberis vulgaris root bark, bryonia alba whole, causticum, citrullus colocynthis fruit pulp, solanum dulcamara top, ferrosoferric phosphate, ledum palustre twig, lycopodium clavatum spore, ranunculus bulbosus, rhododendron aureum leaf, toxicodendron pubescens leaf , and sulfur tablet
- NDC Code(s): 62795-1010-2, 62795-1010-3
- 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 December 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENTS
Each tablet contains: *Arnica montana, radix 6X, *Berberis vulgaris 8X, *Bryonia alba 4X, 8X, 12X, 30X, Causticum 8X, *Colocynthis 5X, *Dulcamara 6X, Ferrum phosphoricum 12X, *Ledum palustre 6X, *Lycopodium clavatum 10X, *Ranunculus bulbosus 6X, *Rhododendron chrysanthum 8X, *Rhus toxicodendron 4X, 8X, 12X, 30X, *Sulphur 10X 15.8 mg each.
*Natural Ingredients
- INACTIVE INGREDIENTS
- PURPOSE
- WARNINGS
- USES
-
Directions
At first sign of symptoms: Adults: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage.
Standard dosage: Adults: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.
For children under 18, consult your health professional.
Allow tablets to dissolve completely in the mouth, do not swallow.
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BHI ARTHRITIS
arnica montana root, berberis vulgaris root bark, bryonia alba whole, causticum, citrullus colocynthis fruit pulp, solanum dulcamara top, ferrosoferric phosphate, ledum palustre twig, lycopodium clavatum spore, ranunculus bulbosus, rhododendron aureum leaf, toxicodendron pubescens leaf , and sulfur tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1010 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT 6 [hp_X] BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 8 [hp_X] BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (BRYONIA ALBA WHOLE - UNII:56K0VVT47P) BRYONIA ALBA WHOLE 4 [hp_X] CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 4 [hp_X] CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17) CITRULLUS COLOCYNTHIS FRUIT PULP 5 [hp_X] SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 6 [hp_X] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 12 [hp_X] LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) LEDUM PALUSTRE TWIG 6 [hp_X] LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 10 [hp_X] RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB) RANUNCULUS BULBOSUS 8 [hp_X] RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U) RHODODENDRON AUREUM LEAF 6 [hp_X] TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF 4 [hp_X] SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 10 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) DEXTROSE (UNII: IY9XDZ35W2) 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:62795-1010-3 1 in 1 CARTON 01/01/2015 1 100 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:62795-1010-2 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/23/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/01/2015 Labeler - MediNatura Inc (079324099) Establishment Name Address ID/FEI Business Operations MediNatura Inc 102783016 manufacture(62795-1010)