FDA.reportPublic FDA data

NoDoz Alertness Aid

Product NDC
66715-9899
11-digit product format
667159899
Labeler code
66715
Product ID
66715-9899_2b0c2bf0-c3da-9d92-e063-6294a90ab8fd
Type
HUMAN OTC DRUG
Nonproprietary name
Caffeine tablet, film-coated
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lil' Drug Store Products, Inc.
Application
M011
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-01-02
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

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
NoDoz Alertness Aid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CAFFEINE200 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3G6A5W338EInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198520Internal RxNorm lookup
795925Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e700e809-29b5-799e-e053-2a95a90a235cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66715-9899-0NoDoz Alertness Aid10 in 1 VIAL, PLASTICTABLET, FILM COATED104
66715-9899-3NoDoz Alertness Aid2 in 1 POUCHTABLET, FILM COATED24
66715-9899-3NoDoz Alertness Aid3 in 1 CARTONTABLET, FILM COATED34
66715-9899-4NoDoz Alertness Aid2 in 1 CARTONTABLET, FILM COATED24
66715-9899-4NoDoz Alertness Aid10 in 1 BLISTER PACKTABLET, FILM COATED104
66715-9899-6NoDoz Alertness Aid1 in 1 CARTONTABLET, FILM COATED14
66715-9899-6NoDoz Alertness Aid60 in 1 BOTTLE, PLASTICTABLET, FILM COATED604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66715-9899NODOZ ALERTNESS AID (CAFFEINE TABLET, FILM-COATED) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC.]4Current NDC, Legacy NDC, 7 package rows20250108_e700e809-29b5-799e-e053-2a95a90a235c.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stay AwakeCAFFEINEAAA Pharmaceutical, Inc.14967dc9-d223-d954-e063-6394a90aa6762024-06-13WarningsExact identifier
application number: M011
JET ALERT Regular StrengthCAFFEINEBell Pharmaceuticals, Inccd7366f9-6ee9-4f1d-bfd2-3ce067f59b2d2023-12-15WarningsExact identifier
application number: M011
Sleep AidDIPHENHYDRAMINE HCLAllegiant Health9746911a-36bc-45eb-adfd-e96439d7a8652021-08-30WarningsExact identifier
application number: M011
Topcare Stay Awake Maximum StrengthCAFFEINETopCo Associates, LLC2223cf52-c172-462d-aacc-b069849b74412021-04-28WarningsExact identifier
application number: M011
Stay AwakeCAFFEINEAllegiant Health959b50a1-3037-4f94-8bc5-6515018150922019-01-08WarningsExact identifier
application number: M011
Stay AwakeCAFFEINEMarc Glassman, Inc.fda5b0a8-2c85-4a8b-97ab-777682c816e22016-12-21WarningsExact identifier
application number: M011

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198520caffeine 200 MG Oral TabletPSNe700e809-29b5-799e-e053-2a95a90a235c4
795925NoDoz 200 MG Oral TabletPSNe700e809-29b5-799e-e053-2a95a90a235c4
795925caffeine 200 MG Oral Tablet [No Doz]SBDe700e809-29b5-799e-e053-2a95a90a235c4
198520caffeine 200 MG Oral TabletSCDe700e809-29b5-799e-e053-2a95a90a235c4
795925No Doz 200 MG Oral TabletSYe700e809-29b5-799e-e053-2a95a90a235c4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66715-9899-06671598990010 TABLET, FILM COATED in 1 VIAL, PLASTIC (66715-9899-0) 2022-09-15NoNoCurrent
66715-9899-3667159899033 POUCH in 1 CARTON (66715-9899-3) / 2 TABLET, FILM COATED in 1 POUCH3 pouch2022-05-240000-00-00NoNoCurrent
66715-9899-4667159899042 BLISTER PACK in 1 CARTON (66715-9899-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK2 blister pack2022-09-150000-00-00NoNoCurrent
66715-9899-6667159899061 BOTTLE, PLASTIC in 1 CARTON (66715-9899-6) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2022-01-020000-00-00NoNoCurrent