VICKS ZZZQUIL SOOTHING SLEEP NIGHTTIME SLEEP-AID- diphenhydramine hcl liquid 
The Procter & Gamble Manufacturing Company

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Vicks ZzzQuil™ SOOTHING SLEEP NIGHTTIME SLEEP-AID

Drug Facts

Active ingredient (in each 30 mL)

Diphenhydramine HCl 50 mg

Purpose

Nighttime sleep-aid

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

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• take only one dose (30 mL) per day (24 hours)
• only use the dose cup provided

adults & children 12 yrs & over30 mL at bedtime
children under 12 yrsdo not use

Other information

Inactive ingredients

anhydrous citric acid, D&C Yellow No. 10, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavors (with chamomile and honey), glycerin, polysorbate 20, propylene glycol, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol, sucralose, water

Questions?

1-877-881-5813

TAMPER EVIDENT: DO NOT USE IF PRINTED SHRINKBAND ON BOTTLE IS BROKEN OR MISSING.

DIST. BY PROCTER & GAMBLE,

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 354 ml Bottle Label

VICKS ®

ZzzQuil™

SOOTHING SLEEP

NIGHTTIME SLEEP-AID

Diphenhydramine HCl

Fall Asleep Fast

Wake Up Refreshed


Chamomile Honey Flavored

Non-Habit Forming

Not for colds or for pain

12 FL OZ (354 ml)

830

VICKS ZZZQUIL  SOOTHING SLEEP NIGHTTIME SLEEP-AID
diphenhydramine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-830
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
HONEY (UNII: Y9H1V576FH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
CHAMOMILE (UNII: FGL3685T2X)  
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorHONEY (Chamomile Honey) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-830-12354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/06/2024
2NDC:69423-830-242 in 1 CARTON02/06/2024
2354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01002/06/2024
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 1/2024
Document Id: 0fdafce6-3f44-dd15-e063-6294a90ad123
Set id: 0f8a8291-7468-735e-e063-6394a90a6643
Version: 2
Effective Time: 20240126
 
The Procter & Gamble Manufacturing Company