Umcka FastActives Cherry

Manufacturer
Schwabe North America, Inc. | ProSolutions, Inc.
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:28:34

Label at a glance#

ProductUmcka FastActives Cherry
Active ingredientPELARGONIUM SIDOIDES ROOT
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

PELARGONIUM SIDOIDES  1X

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CITRIC ACID

MALIC ACID

MALTODEXTRIN

NATURAL FLAVOR

SILICA

XYLITOL

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Tear packet open, pour contents into mouth and swallow.

For best results, use at first sign of symptoms and continue to use for an additional 48 hours after symptoms cease.

Adults and children 13 years of age and older: take contents of 1 packet 3 times daily
Children 6-12 years of age: take contents of 1 packet 2 times daily
Children under 6 years of age: consult a doctor

Indications & Usage

INDICATIONS & USAGE SECTION

Shortens duration and reduces severity of symptoms associated with the common cold and throat/nasal/bronchial irritations: congestion, cough,  hoarseness, sore throat.  

Purpose

OTC - PURPOSE SECTION

Shortens duration and reduces severity of symptoms associated with the common cold and throat/nasal/bronchial irritations: congestion, cough, hoarseness, sore throat.

Warning

WARNINGS SECTION

Sore throat warning: if sore throat is severe, persists more than 2 days, is accompanied or followed by a fever, headache, rash, nausea, or vomiting, consult a doctor pomptly.

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a peristent or chronic cough such as occurs occurs with smoking, asthma, chronic bronchitis, or emphysema, a cough that is accompanied by excessive phlegm (mucus), been taking any medications, an allergy to plant to the Geraniaceae family. 

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if new symptoms occur, symptoms get worse or last more than 7 days, fever worsens or lasts more than 3 days,  cough lasts more than 7 days or occurs with rash or persistent headache.

These could be signs of a serious condition. 

Pregnant or breast feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breast-feeding, ask a healthcare professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdose

OVERDOSAGE SECTION

In case of overdose, seek medical help or contract a Posion Control Center immediatley. 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LGBN60166.02-Umcka-CC-Kid-Cherry-FastActive-10ct.jpgLGBN60166.02-Umcka-CC-Kid-Cherry-FastActive-10ct.jpg

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53499-1166-0Umcka FastActives Cherry700 mg in 1 PACKETPOWDER7008
53499-1166-0Umcka FastActives Cherry10 in 1 CARTONPOWDER108

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53499-1166UMCKA FASTACTIVES CHERRY (PELARGONIUM SIDOIDES) POWDER [SCHWABE NORTH AMERICA, INC.]8Legacy NDC, 2 package rows20241031_2b3aa577-60b0-4855-ad94-312a6ca0677c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
53499-1166-0EA - Each53499-1166fa8f7951-d5d5-46fa-98dd-d665649a6cb312025-10-14

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
53499-116653499-1166-0

Ingredients#

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

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

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
27b85f2a-4799-4c96-aa4d-ade5886415d22b3aa577-60b0-4855-ad94-312a6ca0677c2024-10-29WarningsExact identifier
spl id: 27b85f2a-4799-4c96-aa4d-ade5886415d2
spl set id: 2b3aa577-60b0-4855-ad94-312a6ca0677c

Reported adverse events (FAERS/openFDA)#

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