Diphenhydramine Hydrochloride
12.5 mg/5mL · Solution
- Prescription only
- Histamine-1 Receptor Antagonist
- Active substance
- Diphenhydramine Hydrochloride
- Made by
- PAI Holdings, LLC dba PAI Pharma
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
At a glance
Quoted from the official label · 2024-04-05
Histamine-1 Receptor Antagonist
- Antihistaminic For allergic conjunctivitis due to foods; mild, uncomplicated allergic skin manifestations of urticaria and angioedema; amelioration of allergic reactions to blood or plasma; dermatographism; as…
Adults 25 to 50 mg three to four times daily.
Maximum daily dosage not to exceed 300 mg.
Full directions ↓Use in Neonates or Premature Infants This drug should not be used in neonates or premature infants.
All warnings ↓- Prescription only
- FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-01
Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed
What it is for
Diphenhydramine hydrochloride in the oral form is effective for the following indications:
- Antihistaminic For allergic conjunctivitis due to foods; mild, uncomplicated allergic skin manifestations of urticaria and angioedema; amelioration of allergic reactions to blood or plasma; dermatographism; as therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled.
- Motion Sickness For active and prophylactic treatment of motion sickness.
- Antiparkinsonism For parkinsonism (including drug-induced) in the elderly unable to tolerate more potent agents; mild cases of parkinsonism (including drug-induced) in other age groups; in other cases of parkinsonism (including drug-induced) in combination with centrally acting anticholinergic agents.
- Nighttime Sleep-aid.
From the official label · 2024-04-05 · DailyMed
How it works
From this product’s own US prescribing label.
Diphenhydramine hydrochloride is an antihistamine with anticholinergic (drying) and sedative effects.
Antihistamines appear to compete with histamine for cell receptor sites on effector cells.
Little, if any, is excreted unchanged in the urine; most appears as the degradation products of metabolic transformation in the liver, which are almost completely excreted within 24 hours.
Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2024-04-05
Do not take it if
- Use in Neonates or Premature Infants This drug should not be used in neonates or premature infants.
- Use in Nursing Mothers Because of the higher risk of antihistamines for infants generally, and for neonates and prematures in particular, antihistamine therapy is contraindicated in nursing mothers.
- Antihistamines are also contraindicated in the following conditions Hypersensitivity to diphenhydramine hydrochloride and other antihistamines of similar chemical structure.
Quoted from the official label, section “Contraindications”.
How to take it
These directions are for this exact strength and form. Another one is different.
- DOSAGE SHOULD BE INDIVIDUALIZED ACCORDING TO THE NEEDS AND THE RESPONSE OF THE PATIENT.
- A single oral dose of diphenhydramine hydrochloride is quickly absorbed with maximum activity occurring in approximately one hour.
- The duration of activity following an average dose of diphenhydramine hydrochloride is from four to six hours.
- Adults 25 to 50 mg three to four times daily.
- The nightime sleep aid dosage is 50 mg at bedtime.
- Pediatric Patients, other than premature infants and neonates 12.5 to 25 mg three or four times daily.
- Maximum daily dosage not to exceed 300 mg.
- For physicians who wish to calculate the dose on the basis of body weight or surface area, the recommended dosage is 5 mg/kg/24 hours or 150 mg/m2/24 hours.
- Data are not available on the use of diphenhydramine hydrochloride as a nighttime sleep-aid in
- children under 12 years.
- The basis for determining the most effective dosage regimen will be the response of the patient to medication and the condition under treatment.
- In motion sickness, full dosage is recommended for prophylactic use, the first dose to be given 30 minutes before exposure to motion and similar doses before meals and upon retiring for the duration of exposure
Quoted from the official label, section “Dosage & Administration”.
Other warnings
- Antihistamines should be used with considerable caution in patients with narrow-angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction, symptomatic prostatic hypertrophy, or bladder-neck obstruction.
- Use in Pediatric Patients In pediatric patients, especially, antihistamines in overdosage may cause hallucinations, convulsions, or death.
- As in adults, antihistamines may diminish mental alertness in pediatric patients.
- In the young pediatric patient, particularly, they may produce excitation.
- Use in the Elderly (approximately 60 years or older) Antihistamines are most likely to cause dizziness, sedation, and hypotension in elderly patients.
Quoted from the official label, section “Warnings”.
Pregnancy and breastfeeding
- Pregnancy Category B Reproduction studies have been performed in rats and rabbits at doses up to 5 times the human dose and have revealed no evidence of impaired fertility or harm to the fetus due to diphenhydramine hydrochloride.
- There are, however, no adequate and well-controlled studies in pregnant women.
- Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.
Quoted from the official label, section “OTC — Pregnancy or Breast Feeding”.
Other medicines
Diphenhydramine hydrochloride has additive effects with alcohol and other CNS depressants (hypnotics, sedatives, tranquilizers, etc.). MAO inhibitors prolong and intensify the anticholinergic (drying) effects of antihistamines.
Quoted from the official label, section “Drug Interactions”.
Side effects
- The most frequent adverse reactions are underscored.
- General:
- Urticaria, drug rash, anaphylactic shock, photosensitivity, excessive perspiration, chills, dryness of the mouth, nose and throat.
- Cardiovascular System: Hypotension, headache, palpitations, tachycardia, extrasystoles.
- Hematologic System: Hemolytic anemia, thrombocytopenia, agranulocytosis.
- Nervous System:
- Sedation, sleepiness, dizziness, disturbed coordination , fatigue, confusion, restlessness, excitation, nervousness, tremor, irritability, insomnia, euphoria, paresthesia, blurred vision, diplopia, vertigo, tinnitus, acute labyrinthitis, neuritis, convulsions.
- GI System: Epigastric distress , anorexia, nausea, vomiting, diarrhea, constipation.
- GU System: Urinary frequency, difficult urination, urinary retention, early menses.
- Respiratory System:
- Thickening of bronchial secretions , tightness of chest or throat and wheezing, nasal stuffiness.
- To report SUSPECTED ADVERSE REACTIONS, contact Pharmaceutical Associates, Inc. at 1-800-845-8210 of FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .
Quoted from the official label, section “Adverse Reactions”.
How to store it
Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]. Protect from freezing and light.
Quoted from the official label, section “Storage and Handling”.
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
BulgariaNo exact match for this strength and form
CanadaNo exact match for this strength and form
Details
| Made by | PAI Holdings, LLC dba PAI Pharma |
|---|---|
| Active substance | Diphenhydramine Hydrochloride |
| Used in | Breathing, airways, allergies and cough |
| Strength | 12.5 mg/5mL |
| Form | Solution |
| Route | Oral |
| Packs | 10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE |
| NDC | 0121-0489 |
Source: NDC Directory · 2026-09-13 · not reviewed by a clinician
Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).
Other strengths and forms
65 products are sold under this name. Grouped by form; a number on a strength means several companies make it.
- Capsule21 products
- Injection11 products
- Capsule, Liquid Filled8 products
25 mg3
- Injection, Solution7 products
Show all forms · 8 forms
- Solution6 products
12.5 mg/5mL3
12.5 mg/5mL · 3 companies
- Camber Pharmaceuticals, Inc.
- Oncor Pharmaceuticals
- PAI Holdings, LLC dba PAI Pharma · this page
25 mg/10mL3
25 mg/10mL · 3 companies
- Tablet6 products
25 mg5
- 50 mg
- Tablet, Film Coated4 products
25 mg4
- Tablet, Coated2 products
25 mg2
25 mg · 2 companies
Same active substance
These contain the same substance. That does not mean one can replace another — ask a pharmacist.