HISTAPRIN- diphenhydramine tablet 
NorMed

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HISTAPRIN

Active Ingredient (in each caplet)

Diphenhydramine Hydrochloride 25mg

Purpose:

Antihistamine

Uses:

Temporarily relieves these symptoms due to the common cold, hay fever, or other upper respiratory allergies:

Warnings:

Do not use with any other products containing diphenhydramine, even one used on skin

Ask a doctor before use if you have:

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product:

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

Do not take more than directed

Adults and children 12 years of age and over:

Children under 12 years of age: ask a doctor

Other information:

corn starch, D&C red #27 aluminum lake, dibasic calcium phosphate dihydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, stearic acid, talc, titanium dioxide

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HISTAPRIN 
diphenhydramine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0150
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)  
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (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
ColorpinkScoreno score
ShapeOVALSize11mm
FlavorImprint Code 44;329
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50332-0150-450 in 1 BOX, UNIT-DOSE01/01/2023
11 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01/01/2023
Labeler - NorMed (069560969)

Revised: 1/2024
Document Id: 7e5e918a-b8e5-4c31-98a2-f4af89bd0ed0
Set id: 38786a65-a12b-4479-b63c-b7c15410da04
Version: 1
Effective Time: 20240125
 
NorMed