Home DailyMed ec2070df-8a8a-4cd1-8830-62655433fb3b Benadryl Allergy Ultratab Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Jones Healthcare Group - Packaging Services, Inc | Janssen Cilag SpA
Effective date 2023-11-05
Label type HUMAN OTC DRUG LABEL
Version 6
Source full-release
Hydrated at 2026-05-31 23:59:09 Label at a glance# Product Benadryl Allergy Ultratab
Active ingredient DIPHENHYDRAMINE HYDROCHLORIDE
Label structure 8 sections
Indications and 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 temporarily relieves these symptoms due to the common cold: runny nose sneezing
Dosage and administration take every 4 to 6 hours, or as directed by a doctor do not take more than 6 times in 24 hours adults and children 12 years and over 1 to 2 tablets children 6 to under 12 years 1 tablet children under 6 years do not use
DailyMed RxNorm Mappings# RxCUI, RxNorm string, TTY table RxCUI RxNorm string TTY SPL version 1049632 Benadryl 25 MG Oral Tablet PSN 6 1049630 diphenhydrAMINE HCl 25 MG Oral Tablet PSN 6 1049632 diphenhydramine hydrochloride 25 MG Oral Tablet [Benadryl] SBD 6 1049630 diphenhydramine hydrochloride 25 MG Oral Tablet SCD 6 1049632 Benadryl 25 MG Oral Tablet SY 6 1049632 Benadryl Allergy Ultratab 25 MG Oral Tablet SY 6
DailyMed Pharmacologic Classes# DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67414-226-00 Benadryl Allergy Ultratab 2500 in 1 BOX TABLET, FILM COATED 2500 6 67414-226-00 Benadryl Allergy Ultratab 2 in 1 POUCH TABLET, FILM COATED 2 6 67414-226-54 Benadryl Allergy Ultratab 60 in 1 CARTON TABLET, FILM COATED 60 6 67414-226-54 Benadryl Allergy Ultratab 2 in 1 POUCH TABLET, FILM COATED 2 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67414-226 BENADRYL ALLERGY ULTRATAB (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [JONES HEALTHCARE GROUP - PACKAGING SERVICES, INC] 6 Current NDC, Legacy NDC, 4 package rows 20231106_ec2070df-8a8a-4cd1-8830-62655433fb3b.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 12 matching rows.
Benadryl Allergy Ultratab DIPHENHYDRAMINE HYDROCHLORIDE CARNAUBA WAX CROSCARMELLOSE SODIUM D&C RED NO. 27 ALUMINUM LAKE ANHYDROUS DIBASIC CALCIUM PHOSPHATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED POLYSORBATE 80 TITANIUM DIOXIDE DIPHENHYDRAMINE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 10 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.