Sleep Aid

Manufacturer: Hi-Tech Nutraceuticals, LLC
Effective date: 2026-07-06
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: weekly-update
Hydrated at: 2026-07-17 21:43:39

Label at a glance#

ProductNighttime Sleep Aid

Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE, ACETAMINOPHEN

Label structure17 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

actives

OTC - ASK DOCTOR SECTION

ask a doc

OTC - ASK DOCTOR/PHARMACIST SECTION

ask a doc or pharm

OTC - DO NOT USE SECTION

do not use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach

OTC - PREGNANCY OR BREAST FEEDING SECTION

pregnancy

OTC - PURPOSE SECTION

Purpose

OTC - QUESTIONS SECTION

Questions

OTC - STOP USE SECTION

stop use

OTC - WHEN USING SECTION

when using

OVERDOSAGE SECTION

Overdose

WARNINGS SECTION

warnings

INACTIVE INGREDIENT SECTION

inactives

INDICATIONS & USAGE SECTION

uses

STORAGE AND HANDLING SECTION

storage

DOSAGE & ADMINISTRATION SECTION

directions

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pdp

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1092189	Acetaminophen/diphenhydrAMINE (Oral Pill)	acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet	SCD Active

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69732-005-01	2024-01-30	C162847	48780-1	1030e365-1698-111a-e063-dadaa90a10e2	Sleep Aid
69732-005-01	2024-01-30	C162847	48780-1	1030e365-1698-111a-e063-dadaa90a10e2	Sleep Aid

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Nighttime Sleep Aid
acetaminophen, diphenhydramine
SODIUM STARCH GLYCOLATE TYPE A
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
DIPHENHYDRAMINE HYDROCHLORIDE
DIPHENHYDRAMINE
ACETAMINOPHEN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69732-005	69732-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM STARCH GLYCOLATE TYPE A	H8AV0SQX4D	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
DIPHENHYDRAMINE HYDROCHLORIDE	TC2D6JAD40	ACTIB
ACETAMINOPHEN	362O9ITL9D	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
3	2022-12-31	full-release	2026-05-31 23:52:49

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Nighttime Sleep Aid	ACETAMINOPHEN, DIPHENHYDRAMINE	Hi-Tech Nutraceuticals, LLC	a39e2bd6-3d0a-642b-e053-2995a90a42a0	2026-07-06	Warnings	Exact identifier ndc (package): 69732-005-01 ndc (product): 69732-005 ndc11 (package): 69732000501 spl id: 55f8f71f-4c2c-6161-e063-6394a90a6a8e spl set id: a39e2bd6-3d0a-642b-e053-2995a90a42a0

Reported adverse events (FAERS/openFDA)#

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