Label: SLEEP AID- diphenhydramine hcl tablet, film coated
- NDC Code(s): 11822-0672-6
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 6, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- Purpose
- Uses
-
Warnings
Do not use
- with any other product containing diphenhydramine, even one used on skin
- for children under 12 years of age
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
*Compare to the active ingredient in VICKS®
ZzzQuil® NIGHTTIME SLEEP-AIDNDC 11822-0672-6
SLEEP-AID
DIPHENHYDRAMINE HCl 25 mg
nighttime sleep-aidnot for treating pain, cold or flu
non-habit forming200
CAPLETSACTUAL SIZE
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSINGDISTRIBUTED BY: RITE AID, 200 NEWBERRY COMMONS,
ETTERS, PA 17319
www.riteaid.com
*This product is not manufactured or distributed by The Procter & Gamble Company,
owner of the registered trademark VICKS® ZzzQuil® NIGHTTIME SLEEP-AID.50844 REV0419B67206
SATISFACTION
GUARANTEEif you're not satisfied, we'll
happily refund your money.Rite Aid 44-672
-
INGREDIENTS AND APPEARANCE
SLEEP AID
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0672 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C BLUE NO. 2 ALUMINUM LAKE (UNII: 4AQJ3LG584) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color purple Score no score Shape OVAL Size 14mm Flavor Imprint Code 44;672 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0672-6 200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/24/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M010 07/24/2015 Labeler - Rite Aid Corporation (014578892) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(11822-0672) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(11822-0672) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(11822-0672) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(11822-0672) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(11822-0672)