Rubus

Manufacturer: Marco Pharma International LLC. | Nestmann Pharma GmbH
Effective date: 2026-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 02:36:46

Label at a glance#

ProductRubus

Active ingredientBLACKBERRY, IRIS X GERMANICA ROOT, BILBERRY, SYZYGIUM CUMINI SEED, OKOUBAKA AUBREVILLEI BARK

Label structure2 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Rubus Fruticosus 2xHPUS

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

OTC - PURPOSE SECTION

For temporary relief of pancreatic discomforts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Suggested use

INDICATIONS & USAGE SECTION

Dosage: For acute conditions take 25 drops in water 3-4 times daily. For long-term usage, take 20 drops in water morning and evening.

RECENT MAJOR CHANGES SECTION

Dosage: For acute conditions take 25 drops in water 3-4 times daily. For long-term usage, take 20 drops in water morning and evening.

Warnings

WARNINGS SECTION

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.

DOSAGE & ADMINISTRATION SECTION

(Read Suggested Use Section)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl alcohol (52% by vol.) and Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N18_60986-1011-3-4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
60986-1011-3	2020-12-30	C162847	48780-1	97449f38-c41c-f6ea-e053-dbdaa90aa703	Drug Facts
60986-1011-4	2020-12-30	C162847	48780-1	97449f38-c41c-f6ea-e053-dbdaa90aa703	Drug Facts
60986-1011-3	2019-11-13	C162847	48780-1	97449f38-c41c-f6ea-e053-dbdaa90aa703	Drug Facts
60986-1011-4	2019-11-13	C162847	48780-1	97449f38-c41c-f6ea-e053-dbdaa90aa703	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60986-1011-3	Rubus	50 mL in 1 BOTTLE, GLASS	LIQUID	50		5
60986-1011-4	Rubus	100 mL in 1 PACKAGE	LIQUID	100		5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BILBERRY	ACTIVE INGREDIENT	9P2U39H18W	1
BLACKBERRY	ACTIVE INGREDIENT	8A6OMU3I8L	1
IRIS GERMANICA ROOT	ACTIVE INGREDIENT	8N6VTJ9IWV	1
OKOUBAKA AUBREVILLEI BARK	ACTIVE INGREDIENT	MK2074187Z	1
SYZYGIUM CUMINI SEED	ACTIVE INGREDIENT	820LSF646I	1
BILBERRY	ACTIVE MOIETY	9P2U39H18W	1
BLACKBERRY	ACTIVE MOIETY	8A6OMU3I8L	1
IRIS GERMANICA ROOT	ACTIVE MOIETY	8N6VTJ9IWV	1
OKOUBAKA AUBREVILLEI BARK	ACTIVE MOIETY	MK2074187Z	1
SYZYGIUM CUMINI SEED	ACTIVE MOIETY	820LSF646I	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Rubus
Rubus Fruticosus, Iris Germanica, Vaccinium Myrtillus, Syzygium Jambolanum, Okoubaka Aubrevillei
ALCOHOL
WATER
BLACKBERRY
IRIS X GERMANICA ROOT
BILBERRY
SYZYGIUM CUMINI SEED
OKOUBAKA AUBREVILLEI BARK

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60986-1011	60986-1011-3, 60986-1011-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
BLACKBERRY	8A6OMU3I8L	ACTIB
IRIS X GERMANICA ROOT	8N6VTJ9IWV	ACTIB
BILBERRY	9P2U39H18W	ACTIB
SYZYGIUM CUMINI SEED	820LSF646I	ACTIB
OKOUBAKA AUBREVILLEI BARK	MK2074187Z	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL	3563 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL	3563 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL	3563 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rubus	RUBUS FRUTICOSUS, IRIS GERMANICA, VACCINIUM MYRTILLUS, SYZYGIUM JAMBOLANUM, OKOUBAKA AUBREVILLEI	Marco Pharma International LLC.	bcaf8cd2-3880-4dd7-9895-d33e63c1a229	2026-01-12	Warnings	Exact identifier ndc (package): 60986-1011-3 ndc (package): 60986-1011-4 ndc (product): 60986-1011 ndc11 (package): 60986101103 ndc11 (package): 60986101104 spl id: 483b8e1e-a66f-9470-e063-6294a90af6a3 spl set id: bcaf8cd2-3880-4dd7-9895-d33e63c1a229

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.