Bismuth Magnesite Comp. Special Order

Bismuth Magnesite Comp. Special Order
SPL v2
SPL
SPL Set ID 3d0935dc-cacb-73ec-e054-00144ff88e88
Route
ORAL
Published
Effective Date 2016-09-21
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Bismuth (3 [hp_X]) Antimony Trisulfide (6 [hp_X]) Saffron (1 [hp_X]) Corallium Rubrum Exoskeleton Magnesite Potassium Cation
Inactive Ingredients
Lactose

Identifiers & Packaging

Marketing Status
UNAPPROVED HOMEOPATHIC Active Since 2009-01-09

Description

Directions: FOR ORAL USE ONLY.


Medication Information

Warnings and Precautions

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Indications and Usage

Directions: FOR ORAL USE ONLY.

Dosage and Administration

Take 3-4 times daily. Ages 12 and older:

1/8 teaspoon. Ages 2-11: 1/16 teaspoon.

Under age 2: Consult a doctor.

Description

Directions: FOR ORAL USE ONLY.

Section 50565-1

KEEP OUT OF REACH OF CHILDREN

Section 51727-6

Inactive Ingredient: Lactose

Section 51945-4

Section 53413-1

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

www.urielpharmacy.com

Section 55105-1

Use: Temporary relief of headache.

Section 55106-9

Active Ingredients: Bismuth 3X, Magnesite (Magnesium carbonate) 3X, Antimonite (Antimony trisulfide) 6X, Corallium rubrum (Red coral) 6X,



Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate)6X


Structured Label Content

Indications and Usage (34067-9)

Directions: FOR ORAL USE ONLY.

Dosage and Administration (34068-7)

Take 3-4 times daily. Ages 12 and older:

1/8 teaspoon. Ages 2-11: 1/16 teaspoon.

Under age 2: Consult a doctor.

Warnings and Precautions (34071-1)

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Contains lactose. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Section 50565-1 (50565-1)

KEEP OUT OF REACH OF CHILDREN

Section 51727-6 (51727-6)

Inactive Ingredient: Lactose

Section 51945-4 (51945-4)

Section 53413-1 (53413-1)

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

www.urielpharmacy.com

Section 55105-1 (55105-1)

Use: Temporary relief of headache.

Section 55106-9 (55106-9)

Active Ingredients: Bismuth 3X, Magnesite (Magnesium carbonate) 3X, Antimonite (Antimony trisulfide) 6X, Corallium rubrum (Red coral) 6X,



Crocus sativa (Saffron) 6X, Kalium aceticum (Potassium acetate)6X


Advanced Ingredient Data


Raw Label Data

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