Diphenhydramine HCL
- Dosage form
- CAPSULE
- Labeler
- Preferred Pharmaceuticals, Inc.
- Label updated
- 2026-04-06
- Retrieved
- 2026-09-07
- Active ingredients
- DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient (in each capsule)
Diphenhydramine HCL 25 mg
Diphenhydramine HCL 50 mg
Purpose
Antihistamine
Uses:
-
• Temporarily relieves these symptoms associated with the common cold, hay fever, or other respiratory allergies. -
• Sneezing. -
• Nasal congestion. -
• Runny nose. -
• Itchy, watery eyes.
Do not use
-
• With any other product containing Diphenhydramine HCL, including one applied topically.
Ask a doctor or pharmacist before use
If you have
-
• Trouble urinating due to enlarged prostate gland -
• A breathing problem such as emphysema or chronic bronchitis -
• Glaucoma -
• If you are taking sedatives or tranquilizers
When using this product
-
• Avoid alcoholic drinks. -
• Marked drowsiness may occur. -
• Excitability may occur, especially in children. -
• Alcohol, sedatives and tranquilizers may increase drowsiness. -
• Be careful when driving a motor vehicle or operating machinery.
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.
Directions:
-
• Take every 4-6 hours -
• Do not take more than 6 doses in 24 hours.
|
Adults and children 12 years or over |
1 to 2 capsule |
|
Children 6 to under 12 years |
1 capsule |
|
Children under 6 years |
ask a doctor |
Other information:
-
• Store at room temperature 15-30 degrees C (59-86 degrees F) -
• Protect from excessive moisture
Inactive ingredients: Black Iron Oxide, D & C Red #28, FD & C Blue #1, FD & C Red #40, Gelatin, Lactose Monohydrate, Magnesium Stearate, Silicon Dioxid, Sodium Lauryl Sulfate
Relabeled By: Preferred Pharmaceuticals Inc.
Principal Display Panel
[Image in the official label — see DailyMed source]
Principal Display Panel
[Image in the official label — see DailyMed source]
DailyMed Set ID: 3ac0beba-303d-404e-bfec-0cf8c0e8624d · Version 12
NDC: 68788-9687, 68788-9688