Indications and uses
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes nasal congestion itching of the nose or throat
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes nasal congestion itching of the nose or throat
do not take more than 6 doses in 24 hours adults and children 12 year of age and over take 1 gel every 4 hours children 6 years of age to under 12 years of age take ½ gel every 4 hours children under 6 years of age ask a doctor
Drug Facts
Chlorpheniramine maleate 4 mg
Phenylephrine HCl 10 mg
Antihistamine
Nasal decongestant
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
| adults and children 12 year of age and over | take 1 gel every 4 hours |
| children 6 years of age to under 12 years of age | take ½ gel every 4 hours |
| children under 6 years of age | ask a doctor |
Keep carton for full drug facts.
Store at room temperature 20°-25°C (68°-77°F).
Cherry Flavor (artificial), Citric Acid, Collagen Protein, Color (Red FD&C #40), Glycerin, Granular Sugar, Hydrogenated Starch Hydrolysate, Lubricant (containing one or more of the following: Palm Oil, Coconut Oil, Carnauba Wax, Beeswax), Pectin, Purified Water, Sodium Citrate, Sucralose.
call 1-800-XXX-XXXX
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 42271-200 | 42271-200-15, 42271-200-30, 42271-200-45, 42271-200-60 |
Every source-derived ingredient row is available through these pages.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 8eed2d4d-f40d-02bb-e053-2a95a90a880f | 9f33e21e-c753-46f2-aff5-bd885af697d7 | 2019-07-30 | Warnings | 8eed2d4d-f40d-02bb-e053-2a95a90a880f 9f33e21e-c753-46f2-aff5-bd885af697d7 |
Adverse event summaries are temporarily unavailable. Other product information remains available.