MAX ALLERGY KIDS- diphenhydramine hcl solution 
Akron Pharma Inc.

----------

MAX Allergy Kids
Childrens Allergy
Antihistamine

Diphenhydramine Hydrochloride
12.5mg/5ml Orol Solution
DYE-FREE

Active ingredient (in each 5 mL)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine

Uses

Warnings

Do not use

  • with any other product 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
  • a sodium restricted diet

Ask a doctor or pharmacist before use if the child is

taking sedatives or tranquilizers.

When using this product

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

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

 Age (yr) Dose (mL)
 children 6 to 11 years    5 mL to 10 mL
 children 2 to 5 years    Do not use unless directed by a doctor
 children under 2 years   Do not use

Other information

Inactive ingredients

anhydrous citric acid, bubble gum flavor, purified water, sodium benzoate, sodium citrate, saccharin sodium, sorbitol solution, sucrose.

Questions or comments?

Please Call 1(877) 225-6999

Manufactured for:
Akron Pharma, Inc,
Fairfield, NJ 07004
Manufactured in U.S.A

4
6
8
MAX ALLERGY KIDS 
diphenhydramine hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0023
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Color    Score    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71399-0023-4118 mL in 1 BOTTLE; Type 0: Not a Combination Product11/24/2023
2NDC:71399-0023-8236 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2023
3NDC:71399-0023-6473 mL in 1 BOTTLE; Type 0: Not a Combination Product11/24/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/15/2023
Labeler - Akron Pharma Inc. (067878881)

Revised: 12/2023
Document Id: 8c6097e2-96b6-41e8-8510-964d59c91202
Set id: 96c4ade8-67b1-41e5-8624-fb49090208af
Version: 2
Effective Time: 20231208
 
Akron Pharma Inc.