OTC Medication Information: Sleep Aid NightTime

SLEEP AID NIGHTTIME- diphenhydramine hydrochloride liquid
WinCo Foods, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient (in each 30 mL)

Diphenhydramine HCl 50 mg

Purpose

Nighttime sleep-aid

Uses

  • for the relief of occasional sleeplessness
  • reduces time to fall asleep if you have difficulty falling asleep

Warnings

Do not use

  • with any other product containing diphenhydramine, even one used on the skin
  • for children under 12 years of age
  • with other drugs that cause drowsiness such as antihistamines, nighttime cold/flu products, and other nighttime sleep-aids

Ask a doctor before use if you have

  • a breathing problem such as asthma, emphysema, or chronic bronchitis
  • glaucoma
  • heart disease
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers or any other sleep-aid.

When using this product

  • drowsiness will occur
  • avoid alcoholic beverages and other drugs that cause drowsiness
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

sleeplessness persists 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.

Keep out of reach of children.

Overdose warning: Taking more than directed can cause serious health problems. in case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • take only one dose per day (24 hours) — (see overdose warning)
  • mL= milliliter
  • keep dosing cup with product
  • measure only with dosing cup provided do not use any other dosing device
  • adults and children 12 years and over
    • one dose=30 mL at bedtime if needed, or as directed by a doctor
  • children under 12 years do not use

Other information

  • each 30 mL contains: sodium 23 mg
  • store at 20-25ºC (68-77ºF)
  • do not refrigerate
  • protect from light

Inactive ingredients

citric acid, ethyl alcohol, FD&C blue #1, FD&C red #40, flavor, high fructose corn syrup, polyoxyl 40 stearate, propylene glycol, purified water, saccharin sodium , sodium benzoate, trisodium citrate dihydrate

Questions?

Or to report an adverse event call 800-824-1706 Monday — Friday 9am — 4PM MST

Principal Display Panel

*Compare to the active igredient in ZZZQUIL®

NIGHTTIME

Sleep Aid

DIPHENHYDRAMINE HCI 50 mg / NIGHTTIME SLEEP-AID

Not For Treating Cold or Flu

Safe, Non-Habit Forming

Alcohol 10%

Berry Flavor

FL OZ (mL)

FAILURE TO FOLLOW THESE WARNINGS COULD RESULT IN SERIOUS CONSEQUENCES

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND DOSAGE CUP OR UNDER CAP IS BROKEN OR MISSING.

*This product is not manufactured or distributed byThe Procter & Gamble Company. ZZZQUIL® is a registered trademark of The Procter & Gamble Company.

DISTRIBUTED BY: WINCO FOODS, LLC, BOISE, ID 83704

www.wincofoods.com

Package Label

Diphenhydramine HCI 50 mg
(click image for full-size original)

Winco Foods NightTime Sleep-Aid Berry Flavor

SLEEP AID NIGHTTIME
diphenhydramine hcl liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:67091-290
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 50 mg in 30 mL
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS CITRIC ACID
PROPYLENE GLYCOL
POLYOXYL 40 STEARATE
WATER
SODIUM BENZOATE
SACCHARIN SODIUM ANHYDROUS
TRISODIUM CITRATE DIHYDRATE
HIGH FRUCTOSE CORN SYRUP
FD&C BLUE NO. 1
ALCOHOL
FD&C RED NO. 40
Product Characteristics
Color Score
Shape Size
Flavor BERRY Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:67091-290-17 177 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 06/30/2016
Labeler — WinCo Foods, LLC (056098817)

Revised: 11/2022 WinCo Foods, LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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