ALLERGY RELIEF- diphenhydraime hcl tablet, film coated 
Spirit Pharmaceuticals LLC

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Allergy Relief

Drug Facts

Active Ingredient


Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

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

Warnings

Do not use • to make a 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

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. (1-800-222-1222)

Directions

 adults & children 12 years & over1 to 2 tablets 
 children 6 to under 12 years1 tablet
 children under 6 yearsdo not use this product in children under 6 years of age

Other information

• each tablet contains: calcium 24 mg • store between 15–30°C (59–86°F) • protect from moisture and light

Inactive ingredients

Colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, D&C Red No. 27 Aluminum lake, lecithin, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, talc, titanium dioxide

Questions or comments?

1-888-333-9792

Distributed by:

CABINET HEALTH P.B.C.

Pouch Label

Compare to the active ingredient in: Benadryl® Allergy*

Diphenhydramine HCl 25 mg**

Relieves:
Sneezing
Itchy, Watery Eyes
Runny Nose
Itchy Throat

**May cause drowsiness

Diphenhydramine Jar

ALLERGY RELIEF 
diphenhydraime hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68210-4218
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
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DICALCIUM CITRATE (UNII: LGH2B6RC26)  
D&C RED NO. 27 (UNII: 2LRS185U6K)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorpinkScoreno score
ShapeCAPSULESize11mm
FlavorImprint Code S4
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68210-4218-3300 in 1 JAR; Type 0: Not a Combination Product11/14/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/14/2022
Labeler - Spirit Pharmaceuticals LLC (179621011)

Revised: 12/2023
Document Id: 0bdf3bc9-3714-9494-e063-6394a90a573f
Set id: 99ca3ec9-a28d-4851-951d-34aa982de9d8
Version: 3
Effective Time: 20231206
 
Spirit Pharmaceuticals LLC