Drosera comp. by Uriel Pharmacy Inc. DROSERA COMP. liquid

Drosera comp. by

Drug Labeling and Warnings

Drosera comp. 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 ORAL USE ONLY.

DOSAGE & ADMINISTRATION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

ACTIVE INGREDIENT

Active Ingredients: Drosera (Sundew) 3X, Atropa belladonna (Nightshade) 4X, China (Peruvian bark) 4X, Coccus cacti (Cochineal bug, female) 4X, Helleborus (Christmas rose) 4X, Ipecacuanha (Ipecac) 4X, Mephitis (Secretion from the rectal gland of skunk) 4X, Veratrum (White hellebore) 4X

INACTIVE INGREDIENT

Inactive Ingredients: Distilled water, Organic cane alcohol

PURPOSE

Use: Temporary relief of cough.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN.

WARNINGS

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 conditons or if conditons worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DROSERA COMP. 
drosera comp. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 48951-4009
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ)	DROSERA ROTUNDIFOLIA	3 [hp_X]  in 1 mL
ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H)	ATROPA BELLADONNA	4 [hp_X]  in 1 mL
QUILLAJA SAPONARIA BARK (UNII: 8N0K3807ZW) (QUILLAJA SAPONARIA BARK - UNII:8N0K3807ZW)	QUILLAJA SAPONARIA BARK	4 [hp_X]  in 1 mL
PROTORTONIA CACTI (UNII: LZB7TFX1LT) (PROTORTONIA CACTI - UNII:LZB7TFX1LT)	PROTORTONIA CACTI	4 [hp_X]  in 1 mL
HELLEBORUS FOETIDUS ROOT (UNII: 332Y7EES96) (HELLEBORUS FOETIDUS ROOT - UNII:332Y7EES96)	HELLEBORUS FOETIDUS ROOT	4 [hp_X]  in 1 mL
IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L)	IPECAC	4 [hp_X]  in 1 mL
MEPHITIS MEPHITIS ANAL GLAND FLUID (UNII: 3BN57UN4US) (MEPHITIS MEPHITIS ANAL GLAND FLUID - UNII:3BN57UN4US)	MEPHITIS MEPHITIS ANAL GLAND FLUID	4 [hp_X]  in 1 mL
VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (VERATRUM ALBUM ROOT - UNII:QNS6W5US1Z)	VERATRUM ALBUM ROOT	4 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48951-4009-3	60 mL in 1 BOTTLE, DROPPER; 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(48951-4009)