Indications and uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies sneezing runny nose itchy, watery eyes itching of the nose or throat
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies sneezing runny nose itchy, watery eyes itching of the nose or throat
take every 4 to 6 hours do not take more than 6 doses in 24 hours adults and children 12 years of age and over take 1 to 2 capsules children 6 to under 12 years of age take 1 capsule children under 6 years of age do not use
Diphenhydramine HCl 25 mg
Antihistamine
taking sedatives or tranquilizers.
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 of age and over | take 1 to 2 capsules |
| children 6 to under 12 years of age | take 1 capsule |
| children under 6 years of age | do not use |
butylparaben*, D&C red #28, edible black ink, FD&C blue #1, FD&C red #40, FD&C yellow #6*, gelatin, lactose*, lactose monohydrate*, magnesium stearate*, methylparaben*, polysorbate 80*, propylparaben*, purified water*, sodium lauryl sulphate*, starch
*contains one or more of these ingredients
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
COMPARE TO THE ACTIVE INGREDIENT OF BENADRYL®†
Allergy Relief
Diphenhydramine HCI 25 mg / Antihistamine
Allergy Relief for
CAPSULES
Each capsule individually banded for your protection
**This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Benadryl®.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING OR IF RED BAND AROUND CAPSULE IS BROKEN OR MISSING.
DISTRIBUTED BY:
MIDWOOD BRANDS, LLC
10611 MONROE RD, MATTHEWS, NC 28105
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 55319-481 | 55319-481-01 |
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 |
|---|---|---|---|---|---|---|
| 9025a057-1a30-457d-879d-e66649d2631e | 00a47e41-d836-474c-83a7-83246d7f6a08 | 2021-10-20 | Warnings | 9025a057-1a30-457d-879d-e66649d2631e 00a47e41-d836-474c-83a7-83246d7f6a08 |
Adverse event summaries are temporarily unavailable. Other product information remains available.