Label: SLEEP AID- diphenhydramine hcl liquid
- NDC Code(s): 11673-750-12, 11673-750-24
- Packager: TARGET Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 9, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 30 mL)
- Purpose
- Use
-
Warnings
Do not use
- in 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
- trouble urinating due to an enlarged prostate gland
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to active ingredient in ZzzQuil®*
Nighttime Sleep Aid
50 mg Diphenhydramine HCI per 30 mL
- Non habit-forming
- Not for treating cold or flu
- Alcohol 10%
Berry Flavor
FL OZ (mL)
*This product is not manufactured or distributed by The Procter & Gamble Company. Vicks® ZzzQuil® is a registered trademark of The Procter & Gamble Company.
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.
Distributed by Target Corporation
Minneapolis, MN 55403
- Product Label
-
INGREDIENTS AND APPEARANCE
SLEEP AID
diphenhydramine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-750 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) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE (UNII: 1Q73Q2JULR) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-750-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/31/2023 2 NDC:11673-750-24 2 in 1 PACKAGE 10/31/2023 2 355 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 10/31/2023 Labeler - TARGET Corporation (006961700)