Label: NIGHTTIME SLEEP AID ALCOHOL FREE- diphenhydramine hcl solution
- NDC Code(s): 49035-330-02, 49035-330-45, 49035-330-96
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 14, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 30 mL)
- 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
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
equate™
NDC 49035-330-45
Compare to
VICKS® ZzzQuil®
Nighttime
Sleep-Aid
active
ingredient*Nighttime
Sleep-AidDiphenhydramine HCl
50 mg per 30 mL
Nighttime Sleep-Aid•Non-habit forming
•Not for colds or for pain
• Ages 12+6 FL OZ (177 mL)
Berry Flavor
TAMPER EVIDENT: DO NOT USE IF PRINTED NECK WRAP IS BROKEN OR MISSING
DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716
PRODUCT OF CHINA
*This product is not manufactured or distributed by The Procter &
Gamble Company, owner of the registered trademark VICKS®
ZzzQuil® Nighttime Sleep-Aid. 50844 REV0223C00245Equate 44-002A
-
INGREDIENTS AND APPEARANCE
NIGHTTIME SLEEP AID ALCOHOL FREE
diphenhydramine hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-330 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:49035-330-45 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2016 2 NDC:49035-330-02 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/12/2016 3 NDC:49035-330-96 2 in 1 PACKAGE 09/12/2016 3 355 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 Labeler - Wal-Mart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(49035-330) , pack(49035-330)