UP AND UP CHILDRENS ALLERGY MELTS- diphenhydramine hcl tablet, chewable 
Target Corporation

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up and up children’s allergy melts

Active ingredient (in each tablet)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine

Uses

 temporarily relieves these symptoms due to hay fever or other upper respiratory allergies.
runny nose
itchy, watery eyes
sneezing
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 your doctor before use if you have

a breathing problem such as emphysema or chronic bronchitis
glaucoma
trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers.

When using this product

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

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 at 1-800-222-1222

Directions

find right dose on chart below
Chew one tablet completely at the onset of symptoms. Do not swallow tablets whole.
take every 4 to 6 hours or as directed by a doctor
do not take more than 6 times in 24 hours

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 of age 

1 to 2 chewable tablets (12.5 mg to 25 mg)

adults and children 12 years of age and over

2 to 4 tablets (25 mg to 50 mg)

Other information

store at room temperature. Avoid high humidity. Protect from light

Inactive ingredients

citric acid, crospovidone, D&C Red No. 30, dextrose, FD&C Blue No. 1, flavors, magnesium stearate, maltodextrin, potassium citrate, silica, sodium polystyrene sulfonate, starch, sucralose.

Questions or comments?

 1-866-467-2748

Principal Display Panel

Compare to active ingredient in Children's Benadryl® Allergy Chewables*

Children’s Allergy relief
Diphenhydramine HCl, 12.5 mg/ Antihistamine

For relief of:

sneezing
runny nose
itchy throat
itchy, watery eyes

4-6 Hours/Dose

up & up

Grape Flavor

Naturally and Artificially Flavored

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING

*This product is not manufactured or distributed by Johnson & Johnson Consumer INC, owner of the registered trademark Children's Benadryl® Allergy Chewable Tablets*.


Distributed by Target Corporation

Minneapolis, MN 55403

Made in USA
TM & ©2020 Target Brands, Inc.

100% satisfaction guaranteed or your money back.

Children’s Allergy Grape Flavor 18 Chewable Tablets

up and up childrens allergy melts 18 counts

Children’s Allergy Grape Flavor 48 Chewable Tablets

Childrens Allergy Relief 48 Chewable Tablets
UP AND UP CHILDRENS ALLERGY MELTS 
diphenhydramine hcl tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-012
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK)  
D&C RED NO. 30 (UNII: 2S42T2808B)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)  
STARCH, CORN (UNII: O8232NY3SJ)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorPURPLEScore2 pieces
ShapeROUNDSize16mm
FlavorGRAPEImprint Code RP012
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-012-183 in 1 CARTON11/10/2015
16 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-012-484 in 1 CARTON10/30/2019
212 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/01/2015
Labeler - Target Corporation (006961700)

Revised: 11/2023
Document Id: 6169d155-d6e7-43bd-be65-b6ebd65a61e0
Set id: f98d1d54-8e11-4bb1-825a-ab5447d37847
Version: 9
Effective Time: 20231115
 
Target Corporation