Dosage and administration
adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor
adults and children 12 years of age and over: 1 softgel (50 mg) at bedtime if needed, or as directed by a doctor
Store at room temperature 15°-30°C (59°-86°F) and avoid excessive heat do not use if imprinted safety seal under cap is broken or missing
Drug Facts
Diphenhydramine HCl 50 mg
Nighttime sleep-aid
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers
When using this product avoid alcoholic drinks
Stop use and ask a doctor if sleeplessness persist continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.
If pregnant or breast-feeding, ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
FD&C blue #1, gelatin, glycerin, polyethylene glycol, purified water, sorbitol sorbitan solution and white ink
Call toll free: 1-855-215-8180
MAXIMUM STRENGTH Nighttime Sleep-Aid
200 SOFTGELS
NDC 51013-420-38
*Compare to the active ingredient in Unisom® SleepGels®
| Class | Version | Type | Effective |
|---|---|---|---|
| DIPHENHYDRAMINE Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 3e48c9c4-918d-5d23-2f0b-d2398b06be54 | Product name | 1 | 20140508 |
| 865c72dd-0d94-daac-f728-ddd4ded2a79e | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51013-420-38 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9ef5-d83d-e063-dadaa90ab31f | MAXIMUM STRENGTH Nighttime Sleep-Aid |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51013-420-38 | MAXIMUM STRENGTH Nighttime Sleep Aid | 200 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 200 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 51013-420 | 51013-420-38 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | TC2D6JAD40 | ACTIB |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| GELATIN | 2G86QN327L | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| WATER | 059QF0KO0R | IACT |
| SORBITOL | 506T60A25R | IACT |
| SORBITAN | 6O92ICV9RU | IACT |
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 |
|---|---|---|---|---|---|---|
| f04b1e27-f5b6-42e4-a36c-7a229d24db20 | d1ccefba-f220-4983-b3f5-ca844f2b1bca | 2020-01-03 | Warnings | f04b1e27-f5b6-42e4-a36c-7a229d24db20 d1ccefba-f220-4983-b3f5-ca844f2b1bca |
Adverse event summaries are temporarily unavailable. Other product information remains available.