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

up and up childrens allergy melts by

Drug Labeling and Warnings

up and up childrens allergy melts 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 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

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

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

For relief of:

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

4-6 Hours/Dose

48 Chewable Tablets

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 McNeil Consumer Healthcare, distributor of Children's Benadryl® Allergy FastMelt® Tablets*.

094 04 0063 R01 ID205457
Dist. by Target Corp., Mpls., MN 55403
©2014 Target Brands, Inc.
Shop Target.com

RETAIN CARTON FOR COMPLETE PRODUCT INFORMATION

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Children’s Allergy Grape Flavor 48 Chewable Tablets

INGREDIENTS AND APPEARANCE

UP AND UP CHILDRENS ALLERGY MELTS 
diphenhydramine hcl tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-012
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

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
D&C RED NO. 30 (UNII: 2S42T2808B)
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
Color	PURPLE	Score	2 pieces
Shape	ROUND	Size	16mm
Flavor	GRAPE	Imprint Code	RP012
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-012-18	3 in 1 CARTON	11/10/2015
1		6 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 11673-012-48	4 in 1 CARTON	10/30/2019
2		12 in 1 BLISTER PACK; 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	11/01/2015

Labeler - Target Corporation (006961700)