NoDoz Alertness Aid

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: NoDoz Alertness Aid
Generic name: CAFFEINE TABLET, FILM-COATED
Manufacturer: Lil' Drug Store Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e700e809-29b5-799e-e053-2a95a90a235c
SPL ID: 2b0c2bf0-c3da-9d92-e063-6294a90ab8fd
Version: 4
Effective date: 2025-01-06
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:15

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M011	openfda.application_number
brand name		NoDoz Alertness Aid	openfda.brand_name
generic name		CAFFEINE TABLET, FILM-COATED	openfda.generic_name
manufacturer name		Lil' Drug Store Products, Inc.	openfda.manufacturer_name
ndc	package	66715-9899-0	openfda.package_ndc
ndc	package	66715-9899-6	openfda.package_ndc
ndc	package	66715-9899-4	openfda.package_ndc
ndc	package	66715-9899-3	openfda.package_ndc
ndc	product	66715-9899	openfda.product_ndc
ndc11	package	66715989903	derived:openfda.package_ndc
ndc11	package	66715989904	derived:openfda.package_ndc
ndc11	package	66715989900	derived:openfda.package_ndc
ndc11	package	66715989906	derived:openfda.package_ndc
rxcui		795925	openfda.rxcui
rxcui		198520	openfda.rxcui
spl id		2b0c2bf0-c3da-9d92-e063-6294a90ab8fd	id
spl set id		e700e809-29b5-799e-e053-2a95a90a235c	set_id
unii		3G6A5W338E	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For occasional use only Caffeine warning 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 Do not use in children under 12 years of age as substitute for sleep Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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