GOOD NEIGHBOR PHARMACY Childrens Allergy Relief

DIPHENHYDRAMINE HCL ORAL HUMAN OTC DRUG

GOOD NEIGHBOR PHARMACY Childrens Allergy Relief is an FDA drug label for the active ingredient DIPHENHYDRAMINE HCL manufactured by AMERISOURCE BERGEN administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260713.

Generic name
DIPHENHYDRAMINE HCL
Manufacturer
AMERISOURCE BERGEN
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
46122-798
Application
M012
Label effective
20260713

About this product

GOOD NEIGHBOR PHARMACY Childrens Allergy Relief is an FDA-registered drug product whose active ingredient is DIPHENHYDRAMINE HCL. It is labelled by AMERISOURCE BERGEN taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 46122-798, application M012, label effective 20260713. It is one of 90 FDA drug label records sharing the active ingredient DIPHENHYDRAMINE HCL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing DIPHENHYDRAMINE HCL are most often described in connection with: temporarily relieves, symptoms due, hay fever, upper respiratory, allergies runny, nose itchy, watery eyes, sneezing itching. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient (in each chewable tablet) Diphenhydramine HCl 12.5 mg

Indications & Usage

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

Dosage & Administration

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 Age (Yr) Dose (Chewable tablets) 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 chewable tablets (12.5 mg to 25 mg) adults and children 12 years and over 2 to 4 tablets (25 mg to 50 mg)

Warnings

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 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.

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How products containing DIPHENHYDRAMINE HCL compare

FDA lists 90 drug label records with DIPHENHYDRAMINE HCL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Walgreen Company 7
— — Rite Aid Corporation 6
— — CalmCo LLC 5
— — DOLGENCORP, LLC 5
— — Wal-Mart Stores Inc 5

Recall and safety notices

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-1066-2013 Ifosfamide Injection 3g/60 mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4496-22 AmeriSource Bergen Class II Terminated 20131009
D-1065-2013 Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22 AmeriSource Bergen Class II Terminated 20131009

Frequently asked questions

What is GOOD NEIGHBOR PHARMACY Childrens Allergy Relief used for?
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

Who makes GOOD NEIGHBOR PHARMACY Childrens Allergy Relief?
AMERISOURCE BERGEN is the labeler of record for GOOD NEIGHBOR PHARMACY Childrens Allergy Relief. 90 FDA label records share the active ingredient DIPHENHYDRAMINE HCL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does GOOD NEIGHBOR PHARMACY Childrens Allergy Relief come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is GOOD NEIGHBOR PHARMACY Childrens Allergy Relief prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing DIPHENHYDRAMINE HCL?
Yes. 90 FDA drug label records list DIPHENHYDRAMINE HCL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has GOOD NEIGHBOR PHARMACY Childrens Allergy Relief been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.