DIPHENHYDRAMINE HCL ORAL SOLUTION- diphenhydramine hcl oral solution solution 
Kesin Pharma Corporation

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Diphenhydramine HCl Oral Solution, USP

Drug Facts

Active Ingredients (in each 5 mL)

Diphenhydramine HCl, USP 12.5 mg

Purpose

Antihistamine

Uses

Warnings

Do not use

  • with any other products containing diphenhydramine, even one used on skin
  • to make a child sleepy

Ask a doctor before use if the child has

  • a breathing problem such as chronic bronchitis
  • glaucoma

Ask a doctor or pharmacist before use if the child is taking sedastives or tranquilizers

When using this product

  • marked drowsiness may occur
  • sedatives and tranquilizers may increase drowsiness
  • excitability may occur, especially in children

Keep out of reach of children.

Overdose

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

DIRECTIONS

Age (yr)Doses (mL)
children under 2 yearsdo not use
children 2 to 5 yearsdo not use unless directed by a doctor
children 6 to 11 years5 mL to 10 mL

Other Information

Inactive ingredients

cherry flavor, citric acid, methylparaben, monoammonium glcyrrhizinate, potassium citrate, propylene glycol, polyparaben, purified water, sorbitol, sucralose.

Questions or comments?

1-833-537-4679

*This product is not manufactured by McNeil Consumer Healthcare, distributer of Benadryl Allergy.

Distributed by:

Kesin Pharma

Oldsmar, FL 34677

Revision 02/2025

Kesin Pharma Logo

NDC 81033-029-16

Diphenhydramine HCl

Oral Solution, USP

12.5 mg/5 mL

Antihistamine

Cherry Flavor

16 fl oz. (473 mL)

16 oz Bottle Label

DIPHENHYDRAMINE HCL ORAL SOLUTION 
diphenhydramine hcl oral solution solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81033-029(NDC:84447-103)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HCL (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HCL12.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
METHYLPARABEN (UNII: A2I8C7HI9T)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SORBITOL (UNII: 506T60A25R)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81033-029-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product03/04/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/04/2025
Labeler - Kesin Pharma Corporation (117447816)

Revised: 3/2025
Document Id: 2f871005-de4e-8b2a-e063-6394a90aa43a
Set id: 2f871005-de4d-8b2a-e063-6394a90aa43a
Version: 1
Effective Time: 20250304
 
Kesin Pharma Corporation