KOSHER MEDS CHILDRENS ALLERGY RELIEF- diphenhydramine hcl solution 
Mollec Inc

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Active Ingredient

(in each 5 mL teaspoonful)
Diphenhydramine HCl 12.5mg

Purpose

Antihistamine

Uses

Warnings

Do not use

Ask a doctor before use if the child has

Ask a doctor or pharmacist before use if the child istaking sedatives or tranquilizers

When using this product

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

Directions

 Children under 4 years of age: do not use
 Children 4 to under 6 years of age: do not use unless directed by a doctor
 Children 6 to under 12 years of age: 1 to 2 teaspoonfuls (12.5 mg to 25 mg)

Other Information

Inactive ingredients

Citric acid, D&C Red # 33, FD&C Red # 40, flavor, glycerin, poloxamer 407, purified water, sodium benzoate, sodium chloride, sodium citrate, sucrose

Questions or comments?

Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

Product label

image descriptionimage description

KOSHER MEDS CHILDRENS ALLERGY RELIEF 
diphenhydramine hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82179-004
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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SUCROSE (UNII: C151H8M554)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82179-004-041 in 1 CARTON04/18/2024
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01304/18/2024
Labeler - Mollec Inc (040088196)

Revised: 5/2024
Document Id: 18844590-5a14-4d49-e063-6394a90ae0cf
Set id: 42ad618b-d2e5-4c58-9407-386df4fe4004
Version: 2
Effective Time: 20240515
 
Mollec Inc