Home NDC 82706-019 AXIV Allergy
Product NDC 82706-019
11-digit product format 827060019
Labeler code 82706
Product ID 82706-019_3f023cd0-2567-63dd-e063-6294a90a5dd4
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler VIVUNT PHARMA LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-03-08
Substance DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 25 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 AXIV Allergy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1049909 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82706-019-01 AXIV Allergy 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 4 82706-019-01 AXIV Allergy 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 4 82706-019-02 AXIV Allergy 3 in 1 CARTON CAPSULE, LIQUID FILLED 3 4 82706-019-02 AXIV Allergy 2 in 1 POUCH CAPSULE, LIQUID FILLED 2 4 82706-019-03 AXIV Allergy 25 in 1 CARTON CAPSULE, LIQUID FILLED 25 4 82706-019-03 AXIV Allergy 25 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 25 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82706-019 AXIV ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE, LIQUID FILLED [VIVUNT PHARMA LLC] 3 Current NDC, 6 package rows 20250215_1323a67c-b9c5-038c-e063-6394a90a5e6b.zip
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 74 of 180 · 3,583 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 82706-019-01 82706001901 2 BLISTER PACK in 1 CARTON (82706-019-01) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2024-03-08 No No Current 82706-019-02 82706001902 3 in 1 CARTON Historical 82706-019-03 82706001903 25 BLISTER PACK in 1 CARTON (82706-019-03) / 25 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 25 blister pack 2025-02-12 No No Current