Drug Labeling and Warnings

Drug Details [pdf]

UP AND UP DYE-FREE CHILDRENS ALLERGY- diphenhydramine hydrochloride syrup 
Target Corporation

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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Drug Facts

Active ingredient (in each 5 mL)*

Diphenhydramine HCl USP 12.5 mg

*5mL=one teaspoon

Purpose

Antihistamine

Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itching of the nose or throat

Warnings

Do not use

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

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 sedatives 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.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

  • find right dose on chart below
  • use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.
  • take every 4 to 6 hours
  • do not take more than 6 doses in 24 hours

Age (yr)

Dose (tsp)

children under 2 years

do not use

children 2 to 5 years

do not use unless directed by a doctor

children 6 to 11 years

1 to 2 teaspoonfuls (12.5mg to 25mg)

Attention: use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.

Other information

  • each teaspoon contains: sodium 11 mg
  • store at (59-77°F)
  • do not use if printed inner seal under cap is torn or missing
  • see bottom panel for lot number and expiration date

Inactive ingredients

anhydrous citric acid, carboxymethylcellulose sodium, flavors, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose.

PRINCIPAL DISPLAY PANEL

NDC: 11673-710-12

Compare to active ingredient in Children's
Benadryl® Dye-Free Allergy*

dye-free

children’s allergy syrup

diphenhydramine HCl

oral solution antihistamine

alcohol and sugar free

for relief of:

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

CHERRY FLAVOR
AGES 6-11 YEARS

8 FL OZ (236 mL)

100% satisfaction guaranteed or your money back.

We welcome any questions you may have at Target.com/comments or 1-800-910-6874

Each year we give 5% of our profit to communities, which adds up to more than $4 Million a week. See all the good we do together at Target.com/Community

094 04 0101 R00 ID205457

Distributed by Target Corporation

Minneapolis, MN 55403

®&©2014 Target Brands, Inc.

Shop Target.com

*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Children’s Benadryl® Dye –Free Allergy.

up and up dye-free childrens allergy
UP AND UP DYE-FREE CHILDRENS ALLERGY 
diphenhydramine hydrochloride syrup
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 11673-710
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)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
glycerin (UNII: PDC6A3C0OX)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
water (UNII: 059QF0KO0R)  
sodium benzoate (UNII: OJ245FE5EU)  
sorbitol (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorWHITE (Clear, colorless) Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 11673-710-121 in 1 CARTON09/15/201506/24/2019
1236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34109/15/201506/24/2019
Labeler - Target Corporation (006961700)

Revised: 6/2019
 

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