Label: NIGHTTIME SLEEP AID- diphenhydramine hcl tablet, film coated
- NDC Code(s): 70677-0024-1
- Packager: Strategic Sourcing Services LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 5, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each caplet)
- 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
- for children under 12 years of age
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Sunmark®
COMPARE TO SIMPLY SLEEP®
ACTIVE INGREDIENT*
NDC 70677-0024-1nighttime sleep aid
DIPHENHYDRAMINE HCl 25 mg
Nighttime Sleep-AidHelps you fall asleep
Not for treating Pain, Cold or FluACTUAL
SIZENON-HABIT FORMING
24 CAPLETS
*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the
registered trademark Simply Sleep®.
50844 REV1019A36708Distributed by McKesson Corp., via
Strategic Sourcing Services LLC,
Memphis, TN 38141
© 2003 McKesson Corporation
www.sunmarkbrand.com
Money Back GuaranteeRev. 01/22
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS
OPENED OR IF BLISTER UNIT IS TORN, BROKEN
OR SHOWS ANY SIGNS OF TAMPERINGSunmark 44-367
-
INGREDIENTS AND APPEARANCE
NIGHTTIME SLEEP AID
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-0024 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) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color blue Score no score Shape OVAL Size 11mm Flavor Imprint Code 44;367 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-0024-1 2 in 1 CARTON 06/10/2000 06/14/2024 1 12 in 1 BLISTER PACK; 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 06/10/2000 06/14/2024 Labeler - Strategic Sourcing Services LLC (116956644) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(70677-0024) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(70677-0024) , pack(70677-0024) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(70677-0024) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(70677-0024) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(70677-0024) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(70677-0024)