Home NDC 55910-226 Alert
Product NDC 55910-226
11-digit product format 559100226
Labeler code 55910
Product ID 55910-226_7b0804c8-0e96-47e5-9060-4d5bc717799b
Type HUMAN OTC DRUG
Nonproprietary name Caffeine
Dosage form TABLET
Route ORAL
Labeler DOLGENCORP, LLC
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 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 Alert
Listing expiration 2027-12-31 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# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CAFFEINE ACTIVE INGREDIENT 3G6A5W338E ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 CAFFEINE ACTIVE MOIETY 3G6A5W338E ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT L11K75P92J ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-226 ALERT (CAFFEINE) TABLET [DOLGENCORP, LLC] 21 Current NDC, Legacy NDC, 4 package rows 20250512_9e47eed8-4d0f-4a26-b761-578fb593f025.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 55910-226-21 55910022621 2 BLISTER PACK in 1 CARTON (55910-226-21) / 8 TABLET in 1 BLISTER PACK 2 blister pack 1996-11-21 0000-00-00 No No Current 55910-226-31 55910022631 1 BOTTLE, PLASTIC in 1 CARTON (55910-226-31) / 80 TABLET in 1 BOTTLE, PLASTIC 2023-06-08 No No Current