- Active ingredient(in each 30 mL dose cup)
- Purpose
- Uses
-
Warnings
Do not use
- for children under 12 years of age
- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
-
Directions
- do not take more than directed
- mL = milliliter; TBSP = tablespoon; FL OZ = fluid ounce
- use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.
- take only one dose per day (24 hours)
- adults and children 12 years and over: take 30 mL (2 TBSP) in the dosing cup provided at bedtime if needed or as directed by a doctor
- children under 12 years: do not use
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
WalgreensCompare to Vicks® ZzzQuil® Nighttime Sleep-Aid active ingredient††
NDC 0363-0020-45
Wal-Sleep Z®
DIPHENHYDRAMINE HCl / NIGHTTIME SLEEP AIDNIGHTTIME
ALCOHOL FREE• Non-habit forming
6 FL OZ (177 mL)
BERRY FLAVOR
NOT FOR TREATING COLD OR FLU
TAMPER EVIDENT: DO NOT USE IF PRINTED NECK WRAP IS BROKEN OR MISSING
Walgreens Pharmacist Recommended
Walgreens Pharmacist Survey††This product is not manufactured or distributed by Procter & Gamble, owner of the registered trademark Vicks® ZzzQuil® Nighttime Sleep-Aid.
50844 ORG101700245
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2018 Walgreen Co.44-002A
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INGREDIENTS AND APPEARANCE
WAL-SLEEP Z NIGHTTIME
diphenhydramine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0020 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) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SUCRALOSE (UNII: 96K6UQ3ZD4) SUCROSE (UNII: C151H8M554) XANTHAN GUM (UNII: TTV12P4NEE) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) 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:0363-0020-96 2 in 1 PACKAGE 09/12/2016 1 NDC:0363-0020-02 354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:0363-0020-45 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part338 09/12/2016 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 MANUFACTURE(0363-0020) , PACK(0363-0020)