Home NDC 50844-226 Alert
Product NDC 50844-226
11-digit product format 508440226
Labeler code 50844
Product ID 50844-226_7cfe988f-eb9c-4ad9-b601-da533ac80e4f
Type HUMAN OTC DRUG
Nonproprietary name Caffeine
Dosage form TABLET
Route ORAL
Labeler L.N.K. International, Inc.
Application M011
Marketing category OTC MONOGRAPH DRUG
Marketing start 1996-11-21
Substance CAFFEINE
Active strength 200 mg/1
Pharmacologic classes Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
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 Alert
Brand name suffix Alertness Aid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 200 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3G6A5W338E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198520 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 50844-226-12 AlertAlertness Aid 100 in 1 BOTTLE, PLASTIC TABLET 100 14 50844-226-21 AlertAlertness Aid 2 in 1 CARTON TABLET 2 14 50844-226-21 AlertAlertness Aid 8 in 1 BLISTER PACK TABLET 8 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAFFEINE ACTIVE INGREDIENT 3G6A5W338E ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 CAFFEINE ACTIVE MOIETY 3G6A5W338E ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT L11K75P92J ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 DEXTROSE INACTIVE INGREDIENT IY9XDZ35W2 ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ALERT (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50844-226 ALERT ALERTNESS AID (CAFFEINE) TABLET [L.N.K. INTERNATIONAL, INC.] 13 Current NDC, Legacy NDC, 3 package rows 20240816_4bd13171-78a7-44bb-a6d6-94c6de1f945d.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 3 of 3 · 46 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 50844-226-12 50844022612 100 TABLET in 1 BOTTLE, PLASTIC (50844-226-12) 100 tablet 1996-11-21 No No Current 50844-226-21 50844022621 2 BLISTER PACK in 1 CARTON (50844-226-21) > 8 TABLET in 1 BLISTER PACK 2 blister pack 1996-11-21 0000-00-00 No No Current