BHI Uri-Control RX: Homeopathic Product Information

BHI URI-CONTROL RX- apis mellifera, silver nitrate, atropa belladonna, lytta vesicatoria, causticum, equisetum hyemale, petroselinum crispum, pulsatilla vulgaris, smilax ornata root and turpentine oil 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.

DESCRIPTION

Ingredient name

Potency

Quantity

Final dilution

Apis mellifica

6X

30 mg

7X

Argentum nitricum

6X

30 mg

7X

Belladonna

4X

30 mg

5X

Cantharis

6X

30 mg

7X

Causticum

8X

30 mg

5X

Equisetum hyemale

6X

30 mg

7X

Petroselinum sativum

8X

30 mg

9X

Pulsatilla

6X

30 mg

7X

Sarsaparilla

6X

30 mg

7X

Terebinthina

8X

30 mg

9X

INDICATIONS & USAGE

Uri-Control is a homeopathic drug indicated for the treatment of urinary tract infection, albuminuria, hematuria, incontinence.

DOSAGE AND ADMINISTRATION

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

• Standard Dosage:

Adults and children 12 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours. Children under 12 years: 2 tablets per day, taking 1 tablet every 6 to 8 hours.

• Acute Dosage:

Adults and children 12 years and older: 1 tablet every ½ to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hours. Children under 12 years: 1 tablet every ½ to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 8 tablets in 24 hours.

WARNINGS

Keep out of reach of children.

DOSAGE

300 mg tablets each containing the active ingredients in the strengths listed under Description.

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BHI URI-CONTROL RX
apis mellifera, silver nitrate, atropa belladonna, lytta vesicatoria, causticum, equisetum hyemale, petroselinum crispum, pulsatilla vulgaris, smilax regelii root, and turpentine oil tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50114-9002
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APIS MELLIFERA (APIS MELLIFERA) APIS MELLIFERA 6 [hp_X]
SILVER NITRATE (SILVER CATION) SILVER NITRATE 6 [hp_X]
ATROPA BELLADONNA (ATROPA BELLADONNA) ATROPA BELLADONNA 4 [hp_X]
LYTTA VESICATORIA (LYTTA VESICATORIA) LYTTA VESICATORIA 6 [hp_X]
CAUSTICUM (CAUSTICUM) CAUSTICUM 8 [hp_X]
EQUISETUM HYEMALE (EQUISETUM HYEMALE) EQUISETUM HYEMALE 6 [hp_X]
PETROSELINUM CRISPUM (PETROSELINUM CRISPUM) PETROSELINUM CRISPUM 8 [hp_X]
PULSATILLA VULGARIS (PULSATILLA VULGARIS) PULSATILLA VULGARIS 6 [hp_X]
SMILAX ORNATA ROOT (SMILAX ORNATA ROOT) SMILAX ORNATA ROOT 6 [hp_X]
TURPENTINE OIL (TURPENTINE OIL) TURPENTINE OIL 8 [hp_X]
Inactive Ingredients
Ingredient Name Strength
LACTOSE
MAGNESIUM STEARATE
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:50114-9002-2 1 BOTTLE in 1 CARTON contains a BOTTLE
1 100 TABLET in 1 BOTTLE This package is contained within the CARTON (50114-9002-2)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 01/01/2015
Labeler — MediNatura Inc (102783016)
Establishment
Name Address ID/FEI Operations
MediNatura Inc 102783016 manufacture (50114-9002)

Revised: 10/2019 MediNatura Inc

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