berberis oxalis

berberis oxalis
SPL v5
SPL
SPL Set ID ff96d8ab-3860-443a-8417-c82508e436ff
Route
oral
Published
Effective Date 2025-05-28
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
berberis vulgaris root bark (2 [hp_X]) oxalis stricta whole (3 [hp_X]) saw palmetto (4 [hp_X]) urtica urens (6 [hp_X]) viscum album fruiting top (8 [hp_X]) magnesium cation (10 [hp_X]) bos taurus prostate gland penoxsulam ferric cation
Inactive Ingredients
water sodium chloride

Identifiers & Packaging

Marketing Status
unapproved homeopathic active Since 2009-09-01

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 traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or

persist. If pregnant or nursing, consult a doctor before use.

Active Ingredient

Active Ingredients: Berberis (Barberry) 2X, Oxalis (Wood sorrel) 3X, Sabal serr. (Dwarf palm) 3X, Urtica urens (Small nettle) 3X, Viscum Abietis (Fir tree mistletoe) 4X, Magnesium sulf. (Magnesium sulfate) 6X, Prostata (Bovine prostate gland) 8X, Ferrum picrinicum (Iron picrate) 8X, Granite (Primitive rock containing quartz, feldspar, mica) 10X

Indications and Usage

Directions: FOR ORAL USE ONLY.

Dosage and Administration

Take the contents of one ampule

under the tongue and hold for

30 seconds, then swallow.

Description

Directions: FOR ORAL USE ONLY.

Section 50565-1

KEEP OUT OF REACH OF CHILDREN.

Section 51727-6

Inactive Ingredients: Water, Salt, Lactose

Prepared using rhythmical processes.

Section 51945-4

Section 53413-1

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

shopuriel.com Lot:

Section 55105-1

Use: Temporary relief of headache.


Structured Label Content

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 traces of lactose. Consult a doctor before use for serious conditions or if conditions worsen or

persist. If pregnant or nursing, consult a doctor before use.

Active Ingredient (55106-9)

Active Ingredients: Berberis (Barberry) 2X, Oxalis (Wood sorrel) 3X, Sabal serr. (Dwarf palm) 3X, Urtica urens (Small nettle) 3X, Viscum Abietis (Fir tree mistletoe) 4X, Magnesium sulf. (Magnesium sulfate) 6X, Prostata (Bovine prostate gland) 8X, Ferrum picrinicum (Iron picrate) 8X, Granite (Primitive rock containing quartz, feldspar, mica) 10X

Indications and Usage (34067-9)

Directions: FOR ORAL USE ONLY.

Dosage and Administration (34068-7)

Take the contents of one ampule

under the tongue and hold for

30 seconds, then swallow.

Section 50565-1 (50565-1)

KEEP OUT OF REACH OF CHILDREN.

Section 51727-6 (51727-6)

Inactive Ingredients: Water, Salt, Lactose

Prepared using rhythmical processes.

Section 51945-4 (51945-4)

Section 53413-1 (53413-1)

Questions? Call 866.642.2858

Uriel, East Troy, WI 53120

shopuriel.com Lot:

Section 55105-1 (55105-1)

Use: Temporary relief of headache.


Advanced Ingredient Data


Raw Label Data

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