RUBUS- rubus fruticosus, iris germanica, vaccinium myrtillus, syzygium jambolanum, okoubaka aubrevillei liquid

Rubus by

Drug Labeling and Warnings

Rubus by is a Homeopathic medication manufactured, distributed, or labeled by Marco Pharma International LLC., Nestmann Pharma GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Rubus Fruticosus 2x

Iris Germanica 4xHPUS

Vaccinium Myrtillus 3xHPUS

Syzygium Jambolanum 3xHPUS

Okoubaka Aubrevillei 6xHPUS

The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

Purpose

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Keep out of reach of children.

Suggested use

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Warnings

If pregnant or breast-feeding, consult a health professional before use. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

(Read Suggested Use Section)

Inactive Ingredients

Ethyl Alcohol (52% by vol.) and Water

PRINCIPAL DISPLAY PANEL

MM1

INGREDIENTS AND APPEARANCE

RUBUS 
rubus fruticosus, iris germanica, vaccinium myrtillus, syzygium jambolanum, okoubaka aubrevillei liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60986-1011
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BLACKBERRY (UNII: 8A6OMU3I8L) (BLACKBERRY - UNII:8A6OMU3I8L)	BLACKBERRY	2 [hp_X]  in 100 mL
IRIS GERMANICA ROOT (UNII: 8N6VTJ9IWV) (IRIS GERMANICA ROOT - UNII:8N6VTJ9IWV)	IRIS GERMANICA ROOT	4 [hp_X]  in 100 mL
BILBERRY (UNII: 9P2U39H18W) (BILBERRY - UNII:9P2U39H18W)	BILBERRY	3 [hp_X]  in 100 mL
SYZYGIUM CUMINI SEED (UNII: 820LSF646I) (SYZYGIUM CUMINI SEED - UNII:820LSF646I)	SYZYGIUM CUMINI SEED	3 [hp_X]  in 100 mL
OKOUBAKA AUBREVILLEI BARK (UNII: MK2074187Z) (OKOUBAKA AUBREVILLEI BARK - UNII:MK2074187Z)	OKOUBAKA AUBREVILLEI BARK	6 [hp_X]  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60986-1011-3	50 mL in 1 BOTTLE, GLASS
2	NDC: 60986-1011-4	100 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		03/01/1992

Labeler - Marco Pharma International LLC. (161994277)

Establishment
Name	Address	ID/FEI	Business Operations
Nestmann Pharma GmbH		323426262	manufacture