CHILDREN ALLERGY RELIEF BUBBLEGUM FLAVOR- diphenhydramine hcl liquid

Children Allergy Relief by

Drug Labeling and Warnings

Children Allergy Relief by is a Otc medication manufactured, distributed, or labeled by TARGET CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each 5 mL)

Diphenhydramine HCl USP 12.5 mg

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 at (1-800-222-1222).

Directions

• ▪ find right dose on chart below
• ▪ take every 4 to 6 hours, or as directed by a doctor
• ▪ do not take more than 6 doses in 24 hours 
• ▪ mL = milliliter

• Age (yr):

  Dose (mL)

• 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:

  5 mL to 10 mL

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

Other information

• each 5 mL contains: sodium 15 mg
• store at room temperature
• see bottom panel for lot number and expiration date
• protect from light
• contains low sodium

Inactive ingredients

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

Questions or comments?

1-800-910-6874

Principal display panel

NDC: 11673-832-04

Compare to active ingredient Children’s Benadryl® Dye-Free*

dye-free

children’s allergy relief

diphenhydramine HCl 12.5 mg,

Antihistamine/5 mL Oral Solution

Sugar free

for relief of:

• Runny Nose
• Sneezing
• Itchy, Watery Eyes
• Itchy Throat or Nose

BUBBLEGUM FLAVOR

Naturally and Artificially Flavored

AGES 6+ YEARS

4 FL OZ (118 mL)

100% satisfaction guaranteed or your money back.

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

*This product is not manufactured or distributed by Johnson & Johnson owner of the registered trademark Children’s Benadryl® Dye-Free.

094 04 0378 R01 ID205457

Distributed by Target Corporation

Minneapolis, MN 55403

® & © 2019 Target Brands, Inc.

Shop Taget.com

IMPORTANT: Keep this carton for future reference on full labeling.

DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING

INGREDIENTS AND APPEARANCE

CHILDREN ALLERGY RELIEF  BUBBLEGUM FLAVOR
diphenhydramine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-832
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	12.5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
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
Color		Score
Shape		Size
Flavor	BUBBLE GUM (Naturally and Artificially)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-832-04	1 in 1 CARTON	04/17/2019
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	04/17/2019

Labeler - TARGET CORPORATION (006961700)