Label: WAL-SLEEP Z NIGHTTIME- diphenhydramine hcl solution
- NDC Code(s): 0363-0020-02, 0363-0020-45, 0363-0020-96
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 28, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each 30 mL dose cup)
- Purpose
- Uses
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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
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Directions
- do not take more than directed
- mL = milliliter; 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 at bedtime if needed or as directed by a doctor
- children under 12 years: do not use
- Other information
- Inactive ingredients
- Questions or comments?
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Principal display panel
Walgreens
Compare to Vicks® ZzzQuil® Nighttime
Sleep-Aid active ingredient††NDC 0363-0020-02
Wal-Sleep Z®
DIPHENHYDRAMINE HCI / NIGHTTIME SLEEP AID
NIGHTTIME
ALCOHOL FREE• Non-habit forming
12 FL OZ (355 mL)
NOT FOR TREATING PAIN, COLD OR FLU
BERRY
FLAVORTAMPER EVIDENT: DO NOT USE IF PRINTED
NECK WRAP IS BROKEN OR MISSING††This product is not manufactured or distributed by The
Procter & Gamble Company, owner of the registered
trademark Vicks® ZzzQuil® Nighttime Sleep-Aid.50844 REV1120A00202
Walgreens Pharmacist Recommended
Walgreens Pharmacist SurveyDISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED walgreens.com ©2020 Walgreen Co.Walgreens 44-002
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INGREDIENTS AND APPEARANCE
WAL-SLEEP Z NIGHTTIME
diphenhydramine hcl solutionProduct 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) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SUCRALOSE (UNII: 96K6UQ3ZD4) SUCROSE (UNII: C151H8M554) 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:0363-0020-45 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2016 10/23/2025 2 NDC:0363-0020-02 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2016 10/23/2025 3 NDC:0363-0020-96 2 in 1 PACKAGE 09/12/2016 10/23/2025 3 NDC:0363-0020-02 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M010 09/12/2016 10/23/2025 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(0363-0020) , pack(0363-0020)