gc 714AL (718)

Manufacturer
Geri-Care Pharmaceuticals, Corp
Effective date
2026-08-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-11 03:01:44

Label at a glance#

ProductMUCUS RELIEF
Active ingredientGUAIFENESIN
Label structure9 sections

Indications and uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive to rid the bronchial passageways of bothersome mucus

Dosage and administration

take with full glass of water adults and children 12 years of age and over • take 1 caplet, every 4 hours, while symptoms persist • do not exceed 6 doses in 24 hours children under 12 years of age do not use

Storage and handling

• store in a dry place at 20°C-25°C (68°F-77°F); excursions between 15°-30°C (59°-86°F) • do not expose to heat

Label contents#

Full prescribing information#

Active ingredient (in each caplet)

OTC - ACTIVE INGREDIENT SECTION

Guaifenesin 400 mg

Purpose

OTC - PURPOSE SECTION

Expectorant

Uses

INDICATIONS & USAGE SECTION

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive to rid the bronchial passageways
of bothersome mucus

Warnings

WARNINGS SECTION

Ask a doctor before use if you have

  • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  • cough accompanied by excessive phlegm (mucus)

Stop use and ask a doctor if

  • cough lasts more than 7 days or comes back
  • cough occurs with fever, rash or persistent headache
  • these could be signs of a serious illness.

If pregnant or breast feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take with full glass of water
adults and children 12 years
of age and over
• take 1 caplet, every 4 hours,
while symptoms persist • do
not exceed 6 doses in 24 hours
children under 12 years of agedo not use

Other information

STORAGE AND HANDLING SECTION

• store in a dry place at 20°C-25°C (68°F-77°F); excursions between 15°-30°C (59°-86°F)
• do not expose to heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, dicalcium phosphate dihydrate, maltodextrin, microcrystalline cellulose, povidone, silicon dioxide, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

1-800-540-3765

package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

MUCUS RELIEF

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57896-71857896-718-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
MUCUS RELIEFGUAIFENESINGeri-Care Pharmaceuticals, Corp5afb242f-fac9-dc81-e063-6394a90a84482026-08-27WarningsExact identifier
ndc (package): 57896-718-01
ndc (product): 57896-718
ndc11 (package): 57896071801
spl id: 5afb2444-2f1d-de55-e063-6394a90ad65e
spl set id: 5afb242f-fac9-dc81-e063-6394a90a8448

Reported adverse events (FAERS/openFDA)#

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