Home NDC 68016-683 Allergy Relief
Product NDC 68016-683
11-digit product format 680160683
Labeler code 68016
Product ID 68016-683_2c632d57-d801-46d3-beb6-b7812f177dd7
Type HUMAN OTC DRUG
Nonproprietary name Chlorpheniramine maleate
Dosage form TABLET
Route ORAL
Labeler Chain Drug Consortium
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 1992-12-19
Marketing end 2027-02-28
Substance CHLORPHENIRAMINE MALEATE
Active strength 4 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
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 · 10 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…
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 Allergy Relief Active Ingredients# Ingredient, Strength table Ingredient Strength CHLORPHENIRAMINE MALEATE 4 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V1Q0O9OJ9Z Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1363309 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 68016-683-81 Allergy Relief 1 in 1 CARTON TABLET 1 12 68016-683-81 Allergy Relief 100 in 1 BOTTLE, PLASTIC TABLET 100 12 68016-683-82 Allergy Relief 2 in 1 CARTON TABLET 2 12 68016-683-82 Allergy Relief 12 in 1 BLISTER PACK TABLET 12 12
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68016-683 ALLERGY RELIEF (CHLORPHENIRAMINE MALEATE) TABLET [CHAIN DRUG CONSORTIUM] 11 Current NDC, Legacy NDC, 4 package rows 20241027_34005c55-3176-4f28-9a3b-7dc6fefd01fe.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 Marketing end Sample Exclude flag Status 68016-683-81 68016068381 1 BOTTLE, PLASTIC in 1 CARTON (68016-683-81) / 100 TABLET in 1 BOTTLE, PLASTIC 1992-12-19 2027-02-28 No No Current 68016-683-82 68016068382 2 BLISTER PACK in 1 CARTON (68016-683-82) > 12 TABLET in 1 BLISTER PACK 2 blister pack 1992-12-19 0000-00-00 No No Current