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Up and up childrens allergy melts - Medication Information

Product NDC Code 11673-012
Drug Name

Up and up childrens allergy melts

Type Brand
Pharm Class Histamine H1 Receptor Antagonists [MoA],
Histamine-1 Receptor Antagonist [EPC]
Active Ingredients
Diphenhydramine hydrochloride 12.5 mg/1
Route ORAL
Dosage Form TABLET, CHEWABLE
RxCUI drug identifier 882504
Application Number M012
Labeler Name Target Corporation
Packages
Package NDC Code Description
11673-012-18 3 blister pack in 1 carton (11673-012-18) / 6 tablet, chewable in 1 blister pack
11673-012-48 4 blister pack in 1 carton (11673-012-48) / 12 tablet, chewable in 1 blister pack
11673-012-40 355 ml in 1 bottle (11673-012-40)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Diphenhydramine HCl 12.5 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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)
children under 2 yearsdo not use
children 2 to 5 yearsdo 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)

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
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.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
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

Purpose

Information about the drug product’s indications for use.
Purpose Antihistamine

Spl product data elements

Usually a list of ingredients in a drug product.
up and up childrens allergy melts Diphenhydramine HCl DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE CITRIC ACID MONOHYDRATE CROSPOVIDONE (120 .MU.M) D&C RED NO. 30 FD&C RED NO. 40 DEXTROSE, UNSPECIFIED FORM FD&C BLUE NO. 1 MAGNESIUM STEARATE MALTODEXTRIN POTASSIUM CITRATE SILICON DIOXIDE SODIUM POLYSTYRENE SULFONATE STARCH, CORN SUCRALOSE RP012

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
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 Children’s Allergy Grape Flavor 48 Chewable Tablets Childrens Allergy Relief 48 Chewable Tablets up and up childrens allergy melts 18 counts

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
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 doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use ▪ to make a child sleepy ▪ with any other product containing diphenhydramine, even one used on skin

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
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

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-866-467-2748

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
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

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

Storage and handling

Information about safe storage and handling of the drug product.
Other information • store at room temperature. Avoid high humidity. Protect from light

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API