NIGHTTIME SLEEP AID- diphenhydramine hcl tablet, film coated 
Target Corporation

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Target 44-367

Active ingredient (in each caplet)

Diphenhydramine HCl 25 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

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

avoid alcoholic beverages.

Stop use and ask a doctor if

sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

corn starch, dibasic calcium phosphate dihydrate, FD&C blue #1 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, stearic acid, talc, titanium dioxide

Questions?

Call 1-800-910-6874

Principal Display Panel

Compare to active ingredient in
Simply Sleep®*

NDC 11673-367-12

nighttime sleep aid
diphenhydramine HCI, 25 mg / nighttime sleep aid

non-habit forming

up&up™

100 CAPLETS   

ACTUAL SIZE

100
CAPLETS

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING

100% satisfaction guaranteed
or your money back.

Distributed by Target Corporation
Minneapolis, MN 55403
TM & ©2020 Target Brands, Inc.
50844      REV1019A36712

*This product is not manufactured or distributed
by Johnson & Johnson Corporation, owner of the
registered trademark Simply Sleep®.

Target 44-367

Target 44-367

NIGHTTIME SLEEP AID 
diphenhydramine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-367
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
Inactive Ingredients
Ingredient NameStrength
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
ColorblueScoreno score
ShapeOVALSize11mm
FlavorImprint Code 44;367
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-367-121 in 1 CARTON06/10/2000
1100 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:11673-367-031 in 1 PACKAGE06/10/200005/25/2018
210 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01006/10/2000
Labeler - Target Corporation (006961700)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(11673-367)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(11673-367) , pack(11673-367)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(11673-367)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(11673-367)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(11673-367)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.117025878manufacture(11673-367)

Revised: 7/2023
Document Id: 6f5a0e96-483b-4252-8b0c-9156638e0645
Set id: 2bef39c3-3c1b-4a2d-a8d2-befe4efd2c8c
Version: 15
Effective Time: 20230722
 
Target Corporation