Secale Betula

Secale Betula
SPL v2
SPL
SPL Set ID c7a4db79-e2fd-f524-e053-2a95a90a7a16
Route
ORAL
Published
Effective Date 2021-07-29
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Arnica Montana (12 [hp_X]) Betula Pendula Leaf (3 [hp_X]) Claviceps Purpurea Sclerotium (6 [hp_X]) Lead (8 [hp_X]) Bos Taurus Eye (4 [hp_X]) Betula Pendula Bark Levisticum Officinale Root Tobacco Leaf
Inactive Ingredients
Sodium Chloride Water

Identifiers & Packaging

Marketing Status
UNAPPROVED HOMEOPATHIC Active Since 2009-09-01

Description

Directions: FOR ORAL USE.


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. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Indications and Usage

Directions: FOR ORAL USE.

Dosage and Administration

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Description

Directions: FOR ORAL USE.

Section 50565-1

KEEP OUT OF REACH OF CHILDREN.

Section 51727-6

Inactive Ingredients: Water, Salt

Section 51945-4

Section 53413-1

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

www.urielpharmacy.com Lot:

Section 55105-1

Use: Temporary relief of headache.

Section 55106-9

Active Ingredients: Betula e fol. (Silver birch leaves) 3X, Betula e cort. (Silver birch bark) 4X, Levisticum (Lovage) 6X, Nicotiana (Tobacco) 6X, Secale corn. e grano (Ergot) 6X, Galena (Lead glance) 8X, Retina et chor. (Bovine retina and choroid) 8X, Arnica 12X


Structured Label Content

Indications and Usage (34067-9)

Directions: FOR ORAL USE.

Dosage and Administration (34068-7)

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

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. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Section 50565-1 (50565-1)

KEEP OUT OF REACH OF CHILDREN.

Section 51727-6 (51727-6)

Inactive Ingredients: Water, Salt

Section 51945-4 (51945-4)

Section 53413-1 (53413-1)

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

www.urielpharmacy.com Lot:

Section 55105-1 (55105-1)

Use: Temporary relief of headache.

Section 55106-9 (55106-9)

Active Ingredients: Betula e fol. (Silver birch leaves) 3X, Betula e cort. (Silver birch bark) 4X, Levisticum (Lovage) 6X, Nicotiana (Tobacco) 6X, Secale corn. e grano (Ergot) 6X, Galena (Lead glance) 8X, Retina et chor. (Bovine retina and choroid) 8X, Arnica 12X


Advanced Ingredient Data


Raw Label Data

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