Umcka Cough

Manufacturer
Schwabe North America, Inc. | Schwabe North America
Effective date
2024-04-04
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
legacy-cache
Hydrated at
2026-08-01 21:06:36

Label at a glance#

ProductUmcka Cough ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED , TIN, PELAR...
Active ingredientPELARGONIUM SIDOIDES ROOT, ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, TIN, SPONGIA OFFICINALIS SKELETON, ROASTED
Label structure12 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Pelargonium sidoides 1X

Aconitum napellus 3X

Bryonia 3X 

Hepar sulphuris calcareum 6C

Stannum metallicum 6C

Spongia tosta 3X

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citric Acid

English Ivy Leaf Extract

Ethyl Alcohol 

Glycerin

Lactose Monohydrate

Maltodextrin

Potassium Sorbate

Purified Water

Sorbitol

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, sneezing, stuffy/runny nose.

Temporarily relieves cough due to minor bronchial and throat irritations as may occur with a cold.

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, sneezing, stuffy/runny nose.

Temporarily relieves cough due to minor bronchial and throat irritations as may occur with a cold.

Doage & Administration

DOSAGE & ADMINISTRATION SECTION

Directions

For best results, use at first sign of symptoms.

Continue to use for an additional 48 hours after symptoms cease.

Shake well before each use.

Use only with enclosed dosage cup.

Adults and Children 12 years of age and older:  Take 1 ½ teaspoons (tsp) (7.5 mL) three times daily.

Children 6 to 11 years of age:  Take 1 teaspoon (5 mL) three times daily.

Children under 6 years of age: Consult a physician.

Warnings

WARNINGS SECTION

Sore throat warning:  severe or persistent sore throat for more than 2 days or if accompanied by high fever, headache, nausea, vomiting, or rash may be serious.

Consult a physician promptly.

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a persistent or chronic cough that lasts, is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema, or is accompanied by excessive phlegm (mucus).

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if new symptoms occur, symptoms worsen or do not get better within 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 a sign of a serious condition.

Overdose

OVERDOSAGE SECTION

In case of overdose, seek medical help or contact a Poison Control Center immediately.

Pregnancy or Breast Feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If 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.  

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

15864 Umcka Cough Max Relief.jpg15864 Umcka Cough Max Relief.jpg

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DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53499-5864UMCKA COUGH ACONITUM NAPELLUS, BRYONIA ALBA ROOT, CALCIUM SULFIDE, SPONGIA OFFICINALIS SKELETON, ROASTED , TIN, PELARGONIUM SIDOIDES ROOT (UMCKA COUGH) SYRUP [SCHWABE NORTH AMERICA, INC.]13Legacy NDC20240405_fb2fdf2c-c2f2-4945-a66f-9bd9557ffd42.zip

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53499-586453499-5864-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
5c680f32-524e-4bf7-a2a3-78c9827b3502fb2fdf2c-c2f2-4945-a66f-9bd9557ffd422024-04-04WarningsExact identifier
spl id: 5c680f32-524e-4bf7-a2a3-78c9827b3502
spl set id: fb2fdf2c-c2f2-4945-a66f-9bd9557ffd42

Reported adverse events (FAERS/openFDA)#

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