BHI Bodypure: Homeopathic Product Information

BHI BODYPURE- .alpha.-lipoic acid, avena sativa flowering top, berberis vulgaris root bark, caffeine, cholesterol, juglans regia flowering top, strychnos nux-vomica seed, kerosene, frangula purshiana bark, ricinus communis seed, solidago virgaurea flowering top, urtica urens, viola tricolor and alcohol, x-ray exposed (1000 rad) tablet
MediNatura Inc

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.

ACTIVE INGREDIENT

Each tablet contains: a-Lipoicium acidum 3X, 6X, 8X, *Avena sativa 3X, *Berberis vulgaris 6X, *Caffeinum 6X, *Cholesterinum 10X, *Juglans regia 6X, *Nux vomica 30X, *Petroleum 12X, *Rhamnus purshiana 6X, *Ricinus communis 3X, *Solidago virgaurea 4X, *Urtica urens 6X, *Viola tricolor 4X, *X-Ray 12X 18.8 mg each.

*Natural Ingredients

INACTIVE INGREDIENT

Inactive Ingredients: **Dextrose, ** Lactose, Magnesium Stearate, **Maltodextrin
**contains one or more of these ingredients.

PURPOSE

Cleansing Tablets

Relieves:

• Fatigue

• Headache

• Bloating

USES

For the temporary relief of minor fatigue, headache, bloating

DIRECTIONS

At first sign of symptoms: Adults and children 12 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage.

Standard dosage: Adults and children 12 years and older: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.

For children under 12, consult your health professional.

Allow tablets to dissolve completely in the mouth, do not swallow.

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 known sensitivity to BHI Body Pure or any of its ingredients exists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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BHI BODYPURE
.alpha.-lipoic acid, avena sativa flowering top, berberis vulgaris root bark, caffeine, cholesterol, juglans regia flowering top, strychnos nux-vomica seed, kerosene, frangula purshiana bark, ricinus communis seed, solidago virgaurea flowering top, urtica urens, viola tricolor, and alcohol, x-ray exposed (1000 rad) tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62795-1003
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
.ALPHA.-LIPOIC ACID (.ALPHA.-LIPOIC ACID) .ALPHA.-LIPOIC ACID 3 [hp_X]
AVENA SATIVA FLOWERING TOP (AVENA SATIVA FLOWERING TOP) AVENA SATIVA FLOWERING TOP 3 [hp_X]
BERBERIS VULGARIS ROOT BARK (BERBERIS VULGARIS ROOT BARK) BERBERIS VULGARIS ROOT BARK 6 [hp_X]
CAFFEINE (CAFFEINE) CAFFEINE 6 [hp_X]
CHOLESTEROL (CHOLESTEROL) CHOLESTEROL 10 [hp_X]
JUGLANS REGIA FLOWERING TOP (JUGLANS REGIA FLOWERING TOP) JUGLANS REGIA FLOWERING TOP 6 [hp_X]
STRYCHNOS NUX-VOMICA SEED (STRYCHNOS NUX-VOMICA SEED) STRYCHNOS NUX-VOMICA SEED 30 [hp_X]
KEROSENE (KEROSENE) KEROSENE 12 [hp_X]
FRANGULA PURSHIANA BARK (FRANGULA PURSHIANA BARK) FRANGULA PURSHIANA BARK 6 [hp_X]
RICINUS COMMUNIS SEED (RICINUS COMMUNIS SEED) RICINUS COMMUNIS SEED 3 [hp_X]
SOLIDAGO VIRGAUREA FLOWERING TOP (SOLIDAGO VIRGAUREA FLOWERING TOP) SOLIDAGO VIRGAUREA FLOWERING TOP 4 [hp_X]
URTICA URENS (URTICA URENS) URTICA URENS 6 [hp_X]
VIOLA TRICOLOR (VIOLA TRICOLOR) VIOLA TRICOLOR 4 [hp_X]
ALCOHOL, X-RAY EXPOSED (1000 RAD) (ALCOHOL, X-RAY EXPOSED (1000 RAD)) ALCOHOL, X-RAY EXPOSED (1000 RAD) 12 [hp_X]
Inactive Ingredients
Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE
MALTODEXTRIN
DEXTROSE
Product Characteristics
Color white Score no score
Shape ROUND Size 9mm
Flavor Imprint Code leafman
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62795-1003-3 1 BOTTLE in 1 CARTON contains a BOTTLE
1 100 TABLET in 1 BOTTLE This package is contained within the CARTON (62795-1003-3)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 08/30/2014
Labeler — MediNatura Inc (079324099)
Establishment
Name Address ID/FEI Operations
MediNatura Inc 102783016 manufacture (62795-1003)

Revised: 03/2021 MediNatura Inc

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