4703- Export

Manufacturer: Contract Pharmacal Corp.
Effective date: 2026-08-20
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: daily-update
Hydrated at: 2026-08-25 01:02:13

Label at a glance#

ProductDiphenhydramine Hydrochloride

Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Prestige label

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

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Diphenhydramine Hydrochloride
DIPHENHYDRAMINE
SUCROSE
ANHYDROUS CITRIC ACID
MANNITOL
HYDROXYPROPYL CELLULOSE, UNSPECIFIED
SUCRALOSE
CHERRY
ETHYLCELLULOSES
MICROCRYSTALLINE CELLULOSE
CROSPOVIDONE
D&C RED NO. 7
MAGNESIUM STEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10267-4703	10267-4703-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIPHENHYDRAMINE HYDROCHLORIDE	TC2D6JAD40	ACTIB
SUCROSE	C151H8M554	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
MANNITOL	3OWL53L36A	IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	IACT
SUCRALOSE	96K6UQ3ZD4	IACT
CHERRY	BUC5I9595W	IACT
ETHYLCELLULOSES	7Z8S9VYZ4B	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
CROSPOVIDONE	2S7830E561	IACT
D&C RED NO. 7	ECW0LZ41X8	IACT
MAGNESIUM STEARATE	70097M6I30	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
2	2023-12-01	full-release	2026-06-01 00:03:07

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
5980f4d0-6340-0bb3-e063-6394a90ab029			83713c36-0031-6fa1-e053-2a91aa0a2d11	2026-08-20		Exact identifier spl id: 5980f4d0-6340-0bb3-e063-6394a90ab029 spl set id: 83713c36-0031-6fa1-e053-2a91aa0a2d11

Reported adverse events (FAERS/openFDA)#

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