Indications and uses
temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily relieves sinus congestion and pressure
temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily relieves sinus congestion and pressure
adults and children 12 years and older take 2 tablets every 4 to 6 hours; do not take more than 8 tablets in 24 hours children ages 6 to 12 years take 1 tablet every 4 to 6 hours; do not take more than 4 tablets in 24 hours children under 6 years do not use this product in children under 6 years of age
Pseudoephedrine HCl 30 mg
Nasal decongestant
if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or 2 for 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.
do not exceed recommended dose.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
| adults and
children 12 years and older | take 2 tablets every 4 to
6 hours; do not take more than 8 tablets in 24 hours |
children ages
| take 1 tablet every 4 to 6
hours; do not take more than 4 tablets in 24 hours |
| children under
6 years | do not use this product
in children under 6 years of age |
croscarmellose sodium, dicalcium phosphate, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, silica gel, titanium dioxide, triacetin
(800) 616-2471
DRUG: SudoGest
GENERIC: Pseudoephedrine HCl
DOSAGE: TABLET, FILM COATED
ADMINSTRATION: ORAL
NDC: 70518-0121-0
COLOR: red
SHAPE: ROUND
SCORE: No score
SIZE: 7 mm
IMPRINT: 44;112
PACKAGING: 30 in 1 BOTTLE, PLASTIC
ACTIVE INGREDIENT(S):
INACTIVE INGREDIENT(S):
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0904-5053-24 | EA - Each | 0904-5053 | 5f294304-939e-4c0b-af84-6c0bb2f9bb11 | 1 | 2012-07-24 |
| 0904-5053-59 | EA - Each | 0904-5053 | e6ec7cb2-becd-49b9-bed7-a75f6e1d8887 | 1 | 2012-07-24 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 70518-0121 | 70518-0121-0 |
| 0904-5053 |
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 |
|---|---|---|---|---|---|---|
| 98f0bb19-0056-7f52-e053-2995a90a1528 | edbab9d5-f715-4fe3-adfc-38d7d8d1cea6 | 2019-12-05 | Warnings | edbab9d5-f715-4fe3-adfc-38d7d8d1cea6 |
Adverse event summaries are temporarily unavailable. Other product information remains available.