Label: MEIJER NIGHTTIME SLEEP-AID BERRY FLAVOR- diphenhydramine hydrochloride solution
- NDC Code(s): 41250-738-12
- Packager: MEIJER DISTRIBUTION INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 1, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
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Ask a doctor before use if you have
- ▪
- a breathing problem such as emphysema, or chronic bronchitis
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- glaucoma
- ▪
- difficulty in urination due to enlargement of the prostate gland
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.
When using this product- ▪
- avoid alcoholic beverages
Stop use and ask a doctor if sleeplessness persists continuously for more than two 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.
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Directions
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- take only one dose per day (24 hours)
- ▪
- measure with dosing cup provide
adults & children 12 yrs & over
One Dose = 30 mL at bed time if needed or as directed by a doctor
Children under 12 yrs
do not use
Other information
- •
- each 30 mL dose contains: sodium 23 mg
- •
- store at room temperature
- •
- protect from light. Does not meet USP requirement for light-resistant packaging.
- Inactive ingredients
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PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 12 FL OZ (354 mL Bottle)
meijer®
NDC# 41250-738-12
Compare to Zzzquil® Nighttime Sleep-Aid* active ingredient*
NighttimeSleep-aid
Diphenhydramine HCl 50 mg- •
- Non-Habit Forming
Alcohol-Free
Not for treating Cold or Flu, See Warnings
Berry FlavorNaturally and Artificially Flavored
12 FL OZ (354 mL)MEIJER PHARMACIST RECOMMENED
MONEY BACK GURANTEE
DIST. BY MEIJER DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544
*This product is not manufactured or distributed by The Procter & Gamble Company, owner of the registered trademark ZzzQuil®.
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INGREDIENTS AND APPEARANCE
MEIJER NIGHTTIME SLEEP-AID BERRY FLAVOR
diphenhydramine hydrochloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-738 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 50 mg in 30 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM CITRATE (UNII: EE90ONI6FF) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color PURPLE Score Shape Size Flavor BERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-738-12 354 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M010 03/15/2017 Labeler - MEIJER DISTRIBUTION INC (006959555)