Guaifenesin
- Dosage form
- TABLET
- Labeler
- Health Pharma USA LLC
- Label updated
- 2025-12-05
- Retrieved
- 2026-09-07
- Active ingredients
- GUAIFENESIN
유효 성분
Active ingredient (in each caplet)
Guaifenesin 400 mg
성분·작용
Purpose
Expectorant
효능·용도
Uses
- Temporary symptomatic relief from congested chests and cough.
주의사항
Warnings
A persistent cough may be a sign of a serious condition. If cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache, consult a doctor.
Label information
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).
Label information
When using this product
- Do not exceed recommended dosage.
- Do not consume alcohol, benzodiazepines or opioids.
Label information
Stop use and ask a doctor if
cough lasts for more than 7 days please consult your physician or healthcare provider.
Label information
If pregnant or breast-feeding,ask a health professional before use.
Label information
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
복용법·사용법
Directions
- Adults and children 12 years of age and over:take 1 caplet a day.
- Children under 12 years:Do not use.
- Do not exceed 4 doses in 24 hours.
Label information
Other information
■ Store at 25°C (77°F) excursions between 15°-30°C (59°-86°F).
■ Keep in a dry place and do not expose to heat.
■ Read all product information before use.
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
첨가제
Inactive ingredients
Croscarmellose sodium, Maltodextrin, PVP K30, Silicon dioxide, Microcrystalline cellulose, stearic acid, Purified water.
제조사 문의
Questions or comments?
Call toll free 1-844-832-1138 Monday through Friday 9AM – 5PM EST
PRINCIPAL DISPLAY PANEL
[Image in the official label — see DailyMed source]
[Image in the official label — see DailyMed source]
DailyMed Set ID: 31755594-3e1c-b290-e063-6394a90aba61 · Version 5
NDC: 71679-309