FDA.reportPublic FDA data

NoDoz Alertness Aid

Manufacturer
Lil' Drug Store Products, Inc.
Effective date
2025-01-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:51:01

Label at a glance#

ProductNoDoz Alertness Aid
Active ingredientCAFFEINE
Label structure11 sections

Dosage and administration

Directions adults and children 12 years of age and over: take 1/2 to 1 caplet not more often than every 3 to 4 hours children under 12 years: do not use

Storage and handling

Other information store at 25°C (77°F); excursions permitted between 15°C-30°C (59°F-86°F) see end flap for expiration date and lot number use by expiration date on package

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each caplet)

Caffeine 200 mg

Purpose

OTC - PURPOSE SECTION

Purpose

Alertness aid

Use

INDICATIONS & USAGE SECTION

Use

  • helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Warnings

WARNINGS SECTION

SPL UNCLASSIFIED SECTION

For occasional use only

Caffeine warning

SPL UNCLASSIFIED SECTION

Caffeine warning: The recommended dose of this product contains about as much caffeine as a cup of coffee. Limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and, occasionally, rapid heartbeat.

Do not use

OTC - DO NOT USE SECTION

Do not use

  • in children under 12 years of age
  • as substitute for sleep

OTC - STOP USE SECTION

Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 12 years of age and over: take 1/2 to 1 caplet not more often than every 3 to 4 hours
  • children under 12 years: do not use

Other information

STORAGE AND HANDLING SECTION

Other information

  • store at 25°C (77°F); excursions permitted between 15°C-30°C (59°F-86°F)
  • see end flap for expiration date and lot number
  • use by expiration date on package

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients
corn starch, dextrates hydrated, dibasic calcium phosphate dihydrate, flavor, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

Questions or comments?

call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST) or www.nodoz.com

PDP/Package 60ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fights Fatigue • Max Strength

NoDoz

Aler tness Aid

[caplet image]

60 CAPLETS

200 mg CAFFEINE EACH

CartonCarton

LabelLabel

PDP/Package 6ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fights Fatigue • Max Strength

NoDoz

Aler tness Aid

[caplet image]

200 mg CAFFEINE EACH

6

CAPLETS

3POUCHES, 2 CAPLETS PER POUCH

[Lil' Drug Store logo]

PDP/Package 6ctPDP/Package 6ct

PDP/Package - 20 ct NDC 66715-9899-4

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fights Fatigue • Max Strength

NoDoz

Alertness Aid

[caplet image]

20 CAPLETS

200 mg CAFFEINE EACH

PDP/PackagePDP/Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198520caffeine 200 MG Oral TabletPSN4
795925NoDoz 200 MG Oral TabletPSN4
795925caffeine 200 MG Oral Tablet [No Doz]SBD4
198520caffeine 200 MG Oral TabletSCD4
795925No Doz 200 MG Oral TabletSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66715-989966715-9899-6, 66715-9899-3, 66715-9899-4, 66715-9899-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEO7TSZ97GEPIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
CAFFEINE3G6A5W338EACTIB
STARCH, CORNO8232NY3SJIACT
DEXTRATESG263MI44RUIACT
STEARIC ACID4ELV7Z65APIACT

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NoDoz Alertness AidCAFFEINE TABLET, FILM-COATEDLil' Drug Store Products, Inc.e700e809-29b5-799e-e053-2a95a90a235c2025-01-06WarningsExact identifier
ndc (package): 66715-9899-0
ndc (package): 66715-9899-6
ndc (package): 66715-9899-4
ndc (package): 66715-9899-3
ndc (product): 66715-9899
ndc11 (package): 66715989903
ndc11 (package): 66715989904
ndc11 (package): 66715989900
ndc11 (package): 66715989906
spl id: 2b0c2bf0-c3da-9d92-e063-6294a90ab8fd
spl set id: e700e809-29b5-799e-e053-2a95a90a235c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.