CHILDRENS ALLERGY RELIEF- antihistamine liquid 
Mckesson

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Sunmark Childrens allergy relief dye-free bubblegum flavor

Active ingredient (in each 5 mL tsp)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine

Uses

Warnings

Do not use

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

Ask adoctor before use if you have

  • glaucoma
  • a breathing problem such as emphysema or chronic bronchitis
  • difficulty in urination due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

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

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.

Directions

 Age (yr)Dose (mL or tsp) 
 children under 2 years do not use
 children under 6 years ask a doctor
 children 6 to under 12 years 1 to 2 tsp (5 mL to 10 mL)
 adults and children 12 years and above 2 to 4 tsp (10 mL to 20 mL)

Other information

Inactive ingredients

carboxymethylcellulose sodium, citric acid, flavors, glycerin, purified water, saccharin sodium, sodium benzoate, sorbitol

PDP

Sunmark

Compare to childrens benadyl active ingredient

Children's allergy relief dye-free

antihistamine

Relieves sneezing, runny nose, itchy, watery eyes, itchy throat

Diphenhydramine HCl

antihistamine

Bubblegum Flavor

4 fl oz (118mL)

SN

CHILDRENS ALLERGY RELIEF 
antihistamine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-056
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
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
Colorwhite (clear) Score    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-056-341 in 1 CARTON
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/08/2013
Labeler - Mckesson (177667227)

Revised: 10/2014
Document Id: ea16aeba-89fc-4246-b244-4c3f1b267791
Set id: 4609efc1-71d3-401e-b5f6-0caf48e8670f
Version: 1
Effective Time: 20141027
 
Mckesson