Mucolyte
- Dosage form
- LIQUID
- Labeler
- Rising Pharma Holdings, Inc.
- Label updated
- 2025-12-08
- Retrieved
- 2026-09-07
- Active ingredients
- GUAIFENESIN
Drug Facts
Active Ingredient (in each 5mL)
Guaifenesin, USP 100 mg
Purpose
Expectorant
효능·용도
Uses
- helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.
주의사항
Warnings
Do not use
- if you ever had an allergic reaction to any of the ingredients in this product
Ask a doctor before use if you have
- cough that occurs with too much phlegm (mucus)
- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
Stop use and ask a doctor if
- cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
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 right away.
복용법·사용법
Directions
- Do not take more than 6 doses in a 24-hour period
- Do not exceed recommended dose
| adults and children 12 years and over | 2 to 4 teaspoonfuls (10mL to 20mL) every 4 hours |
| children under 12 years | ask a doctor |
Other Information
- TAMPER-EVIDENT: Do not use if foil seal over bottle opening is torn, broken, or missing.
- store at 20°-25°C (68°-77°F)
- protect from freezing
- protect from light
Inactive Ingredients
Cherry flavor, citric acid, FD&C Red #40, glycerin, menthol, propylene glycol, sodium benzoate, sodium citrate, sodium saccharin, sorbitol, sucralose, water.
Questions or comments
Call 1-844-474-7464
Label information
*This product is neither manufactured nor distributed by the owner of the registered trademark Robitussin®
MUCOLYTETM is a trademark owned by Rising Pharma Holdings, Inc.
Distributed by:
Rising Pharma Holdings, Inc.
East Brunswick, NJ 08816
포장 표시
[Image in the official label — see DailyMed source]
DailyMed Set ID: e4091aaf-44e3-4701-9986-aff248a2f1b8 · Version 1
NDC: 57237-359