FDA.reportPublic FDA data

Umcka Fastactv Berry

Manufacturer
ProSolutions Inc | Schwabe North America, Inc.
Effective date
2025-04-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:13

Label at a glance#

ProductUmcka Fastactv Berry
Active ingredientEUCALYPTUS GLOBULUS LEAF, PHOSPHORUS, IPECAC, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, PELARGONIUM SIDOIDES ROOT, ACONITUM NAPELLUS
Label structure13 sections

Label contents#

Full prescribing information#

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Inactive ingredients panelInactive ingredients panel

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Recent Major Changes

RECENT MAJOR CHANGES SECTION

Dosage & Administration, Warnings, Indications and Usage, added for initial submission in 12/2022.

When expiring marketing dates in version 2, SPL could not find original file file name that included an & in file name.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients panelActive Ingredients panel

Warnings

WARNINGS SECTION

Warnings panelWarnings panel

Ask a Doctor

OTC - ASK DOCTOR SECTION

Ask a Doctor panelAsk a Doctor panel

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdosage

OVERDOSAGE SECTION

Overdose panelOverdose panel

Indications and Usage

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Stop Use

OTC - STOP USE SECTION

Stop use panelStop use panel

Pregnancy or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnancy or breast feeding panelPregnancy or breast feeding panel

Purpose

OTC - PURPOSE SECTION

Purpose and IndicationsPurpose and Indications

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83102-9349-0Umcka Fastactv Berry10 in 1 CARTONPOWDER102
83102-9349-0Umcka Fastactv Berry1 in 1 PACKETPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83102-9349UMCKA FASTACTV BERRY (PELARGONUIM SIDOIDES, ACONITUM NAPELLUS, EUCALYPTUS GLOBULUS, BRYONIA, EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, ALPHA CF) POWDER [PROSOLUTIONS INC]2Current NDC, Legacy NDC, 2 package rows20250411_eedab4b9-509b-3fe5-e053-2995a90a2027.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83102-934983102-9349-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
MALTODEXTRIN7CVR7L4A2DIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6ACTIB
ALCOHOL3K9958V90MIACT
XYLITOLVCQ006KQ1EIACT
PHOSPHORUS27YLU75U4WACTIB
IPECAC62I3C8233LACTIB
SILICON DIOXIDEETJ7Z6XBU4IACT
MALIC ACID817L1N4CKPIACT
BRYONIA ALBA ROOTT7J046YI2BACTIB
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PELARGONIUM SIDOIDES ROOTH6J53HEX8EACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Umcka Fastactv BerryPELARGONUIM SIDOIDES, ACONITUM NAPELLUS, EUCALYPTUS GLOBULUS, BRYONIA, EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, PHOSPHORUS, ALPHA CFProSolutions Inceedab4b9-509b-3fe5-e053-2995a90a20272025-04-10WarningsExact identifier
ndc (package): 83102-9349-0
ndc (product): 83102-9349
ndc11 (package): 83102934900
spl id: 326cc6c1-1604-3317-e063-6394a90a84b4
spl set id: eedab4b9-509b-3fe5-e053-2995a90a2027

Reported adverse events (FAERS/openFDA)#

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