ALLERGY RELIEF DIPHENHYDRAMINE HCI, 25 MG ANTIHISTAMINE- diphenhydramine hcl bar, chewable 
MEIJER DISTRIBUTION, INC.

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Allergy Relief DIPHENHYDRAMINE HCI, 25 mg Antihistamine

Active ingredient (in each piece)

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: 
  •     runny nose
  •     itchy, watery eyes
  •     sneezing
  •     itching of the nose or throat
  • temporarily relieves these symptoms due to the common cold:
  •     runny nose
  •     sneezing

Warnings

Do not use

  • To make child sleepy
  • 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

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product

  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

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 (1-800-222-1222) right away. 

Directions

  • take every 4 to 6 hours, or as directed by a doctor
  • do not take more than 6 times in 24 hour                                                                                                                                                   

    Age (yr)

    Dose (Piece)

    Adults and children 12 years and over

    1 to 2 Pieces (25 mg to 50 mg)

    Children 6 to 11 years

    1 Piece (25 mg)

    Children under 6 years

    Do not use


Other information

  • each piece: contains sodium 9 mg.

very low sodium

  • store in a cool dry place between 20-25°C (68-77°F).
  • Child Resistant Container; do not use if printed seal under cap is broken or missing.

Inactive ingredients:

citric acid, FD&C red #40, flavor, glucose syrup, hydroxypropyl betadex, magnesium stearate, maltitol solution, maltodextrin, neotame, purified water, seaweed extract (carrageenan), sodium chloride, starch, sucralose, sucrose, trisodium citrate dihydrate.

Questions or comments?

Call 1-800-227-6151

Principal display Panel-25 mg carton label

NDC 79481-0700-1

Compare to the active ingredient in Benadryl ® Allergy*

SOFT CHEWS

allergy relief  Diphenhydramine HCl, 25 mg | Antihistamine

RELIEF OF:                    

Sneezing; Itchy, Watery Eyes; Runny Nose & Itchy Throat

10 Pieces                             actual size         

Bubble Gum Flavor                Chewy Bites                   

Principal display Panel-25 mg carton label

ALLERGY RELIEF DIPHENHYDRAMINE HCI, 25 MG ANTIHISTAMINE 
diphenhydramine hcl bar, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79481-0700
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
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
CORN SYRUP (UNII: 9G5L16BK6N)  
HYDROXYPROPYL BETADEX (UNII: 1I96OHX6EK)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTITOL (UNII: D65DG142WK)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
NEOTAME (UNII: VJ597D52EX)  
WATER (UNII: 059QF0KO0R)  
CARRAGEENAN (UNII: 5C69YCD2YJ)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
STARCH, CORN (UNII: O8232NY3SJ)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SUCROSE (UNII: C151H8M554)  
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
Product Characteristics
Colorpink (Light pink to red pink) Scoreno score
ShapeRECTANGLESize23mm
FlavorBUBBLE GUMImprint Code O
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79481-0700-11 in 1 CARTON11/16/202112/29/2023
110 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/16/202112/29/2023
Labeler - MEIJER DISTRIBUTION, INC. (006959555)
Establishment
NameAddressID/FEIBusiness Operations
USpharma Ltd080664601manufacture(79481-0700) , pack(79481-0700)

Revised: 1/2024
 
MEIJER DISTRIBUTION, INC.