FDA.reportPublic FDA data

Umcka FastActives Cherry

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 FastActives Cherry
Active ingredientPELARGONIUM SIDOIDES ROOT
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients panelInactive Ingredients panel

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage and Administration panelDosage and Administration panel

Indications and Usage panel

INDICATIONS & USAGE SECTION

Indications and Usage panelIndications and Usage panel

Warnings panel

WARNINGS SECTION

Warnings panelWarnings panel

Ask a Doctor panel

OTC - ASK DOCTOR SECTION

Ask a Doctor panelAsk a Doctor panel

Stop Use panel

OTC - STOP USE SECTION

Stop Use panelStop Use panel

Pregnancy or Breast Feeding panel

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnancy or Breast Feeding panelPregnancy or Breast Feeding panel

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.Keep out of reach of children.

Over dosage

OVERDOSAGE SECTION

Over dosage panel.Over dosage panel.

Purpose panel

OTC - PURPOSE SECTION

Purpose panelPurpose panel

Package panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package panelPackage panel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83102-1166-0Umcka FastActives Cherry10 in 1 CARTONPOWDER102
83102-1166-0Umcka FastActives Cherry700 mg in 1 PACKETPOWDER7002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83102-1166UMCKA FASTACTIVES CHERRY (PELARGONIUM SIDOIDES) POWDER [PROSOLUTIONS INC.]22 package rows20250411_f5751a54-dca0-0aa4-e053-2995a90a2eb3.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83102-116683102-1166-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICON DIOXIDEETJ7Z6XBU4IACT
XYLITOLVCQ006KQ1EIACT
MALIC ACID817L1N4CKPIACT
MALTODEXTRIN7CVR7L4A2DIACT
PELARGONIUM SIDOIDES ROOTH6J53HEX8EACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
326cc922-9f5d-239e-e063-6394a90a61cdf5751a54-dca0-0aa4-e053-2995a90a2eb32025-04-10WarningsExact identifier
spl id: 326cc922-9f5d-239e-e063-6394a90a61cd
spl set id: f5751a54-dca0-0aa4-e053-2995a90a2eb3

Reported adverse events (FAERS/openFDA)#

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