Muca Clear

Manufacturer
Schwabe North America, Inc
Effective date
2024-10-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:25:46

Label at a glance#

ProductMuca Clear
Active ingredientGUAIFENESIN
Label structure9 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Guaifenesin 200 mg

Inactive Ingredient

INACTIVE INGREDIENT SECTION

carnauba wax

cellulose

dextrin

fenugreek (Trigonella foenum-graecum) (seed) extract

glycerin

hypromellose

magnesium stearate

maltodextrin

marshmallow (Althaea officinalis) (root) extract

mullein (Verbascum thapsus) (leaf) extract

povidone

silica

sodium croscarmellose

stearic acid

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Adults & children 12 years of age and older:  Take 1-2 tablets every 4 hours, not to exceed 12 tablets in 24 hours.

Children 6 - 11 years of age: Take ½ - 1 tablet every 4 hours not to exceed 6 tablets in 24 hours.

Children under 6 years of age: Consult a doctor before use.

Purpose

OTC - PURPOSE SECTION

Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.

Indications & Usage

INDICATIONS & USAGE SECTION

Helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of mucus and make coughs more productive.

Warnings

WARNINGS SECTION

Do not use this product if you are pregnant, attempting to be pregant, or breast-feeding.

Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or where cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if cough persists more than one week, tends to recur, or is accompanied by a fever, rash, or persistent headache.

A persistent cough may be a sign of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdosage

OVERDOSAGE SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LZP13653.H02-Muca-Clear-(OTC)-100-tabs.jpgLZP13653.H02-Muca-Clear-(OTC)-100-tabs.jpg

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59800-1365MUCA CLEAR (GUAIFENESIN) TABLET [SCHWABE NORTH AMERICA, INC]6Legacy NDC20241017_735128ad-6844-4a8e-83d0-29cbb5d66f4a.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59800-136559800-1365-1

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
4a6ccf9b-8b9c-4188-bd2f-a0ac0c285ab9735128ad-6844-4a8e-83d0-29cbb5d66f4a2025-10-20WarningsExact identifier
spl set id: 735128ad-6844-4a8e-83d0-29cbb5d66f4a

Reported adverse events (FAERS/openFDA)#

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