Home NDC 44224-1276 After Bite Xtra
Product NDC 44224-1276
11-digit product format 442241276
Labeler code 44224
Product ID 44224-1276_5ccc1abc-d46b-94ca-e063-6394a90a185f
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl
Dosage form GEL
Route TOPICAL
Labeler Tender Corporation d/b/a Adventure Ready Brands
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-01
Substance DIPHENHYDRAMINE HYDROCHLORIDE
Active strength .4 g/20g
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base After Bite Xtra
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE .4 g/20g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44224-1276-0 After Bite Xtra 1 g in 1 TUBE GEL 1 2 44224-1276-1 After Bite Xtra 1 in 1 BOX GEL 1 2
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 97 of 151 · 3,010 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 44224-1276-0 44224127600 1 g in 1 TUBE 1 g Historical 44224-1276-1 44224127601 1 TUBE in 1 BOX (44224-1276-1) / 1 g in 1 TUBE (44224-1276-0) 1 tube 2025-01-01 No No Current