Bambusa Argentum by Uriel Pharmacy Inc. BAMBUSA ARGENTUM gel

Bambusa Argentum by

Drug Labeling and Warnings

Bambusa Argentum by is a Homeopathic medication manufactured, distributed, or labeled by Uriel Pharmacy Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION

Apply to skin as needed. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Bambusa (Bamboo) 8X, Betonica (Wood betony) 8X, Rosmarinus (Rosemary) 8X, Aurum met. (Metallic gold) 9X, Disci intervert. (Bovine intervertebral discs of the cervical, thoracic and lumbar spine) 10X, Cuprum met. (Copper) 11X, Jasper (Semiprecious stone) 19X, Argentum met. (Silver) 22X, Arnica 22X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Sodium alginate, Lavender oil, Glycerin, Sorbic Acid, Tea tree oil, Grapefruit seed extract

PURPOSE

Use: Temporary relief of headache.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

Warnings: FOR EXTERNAL USE ONLY.
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, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing. Avoid contact with eyes.

QUESTIONS

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BAMBUSA ARGENTUM 
bambusa argentum gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-2138
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK) (BAMBUSA VULGARIS WHOLE - UNII:WCD45M1BSK)	BAMBUSA VULGARIS WHOLE	8 [hp_X]  in 1 g
STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N)	STACHYS OFFICINALIS	8 [hp_X]  in 1 g
ROSMARINUS OFFICINALIS FLOWERING TOP (UNII: 8JM482TI79) (ROSMARINUS OFFICINALIS FLOWERING TOP - UNII:8JM482TI79)	ROSMARINUS OFFICINALIS FLOWERING TOP	8 [hp_X]  in 1 g
GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO)	GOLD	9 [hp_X]  in 1 g
BOS TAURUS INTERVERTEBRAL DISC (UNII: 0A04Z76C13) (BOS TAURUS INTERVERTEBRAL DISC - UNII:0A04Z76C13)	BOS TAURUS INTERVERTEBRAL DISC	10 [hp_X]  in 1 g
COPPER (UNII: 789U1901C5) (COPPER - UNII:789U1901C5)	COPPER	11 [hp_X]  in 1 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	19 [hp_X]  in 1 g
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	22 [hp_X]  in 1 g
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	22 [hp_X]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
LAVENDER OIL (UNII: ZBP1YXW0H8)
GLYCERIN (UNII: PDC6A3C0OX)
SORBIC ACID (UNII: X045WJ989B)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-2138-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Establishment
Name	Address	ID/FEI	Business Operations
Uriel Pharmacy Inc.		043471163	manufacture(48951-2138)