Label at a glance#

ProductEach Relief Equate

Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE

Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose
Diphenhydramine HCI 2%................Topical analgesic

INDICATIONS & USAGE SECTION

Uses Temporarily relieves pain due to: • minor burns • insect bites • sunburn • minor skin irritations • minor cuts • scrapes • rashes due to poison ivy, poison oak & poison sumac

WARNINGS SECTION

Warnings
For external use only.
Do not use • on large areas of the body • with any other product containing diphenhydramine, even one taken by mouth
When using this product • avoid contact with the eyes
Stop use and ask doctor if • condition gets worse • symptoms last more than 7 days • symptoms clear up and occur again in a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions • do not use more than directed • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Camphor, Citric Acid, Diazolidinyl
Urea, Glycerin, Hydroxypropyl Methylcellulose, Methylparaben,
Propylene Glycol, Propylparaben, SD Alcohol 38-B, Sodium
Citrate, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1049880	diphenhydrAMINE (Topical)	diphenhydramine hydrochloride 0.02 MG/MG Topical Gel	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1049880	diphenhydrAMINE HCl 2 % Topical Gel	PSN	1
1049880	diphenhydramine hydrochloride 0.02 MG/MG Topical Gel	SCD	1
1049880	diphenhydramine hydrochloride 2 % Topical Gel	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
DIPHENHYDRAMINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
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
49035-246-03	2020-01-31	C162847	48780-1	9d75b9d0-9cf7-f424-e053-dadaa90a57ce	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-246-03	Each ReliefEquate	103 mL in 1 TUBE	GEL	103		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-246	EACH RELIEF EQUATE (DIPHENHYDRAMINE HCI 2%) GEL [WALMART]	1	Legacy NDC, 1 package rows	20170403_60e242bf-10e5-4627-a75d-b61c5302fbbb.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Each Relief Equate
Diphenhydramine HCI 2%
DIPHENHYDRAMINE HYDROCHLORIDE
DIPHENHYDRAMINE
CAMPHOR (SYNTHETIC)
CITRIC ACID MONOHYDRATE
Diazolidinyl Urea
Glycerin
HYPROMELLOSE, UNSPECIFIED
Methylparaben
Propylene Glycol
Propylparaben
ALCOHOL
Sodium Citrate
Water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
49035-246	49035-246-03

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
CAMPHOR (SYNTHETIC)	5TJD82A1ET	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
Diazolidinyl Urea	H5RIZ3MPW4	IACT
Glycerin	PDC6A3C0OX	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
Methylparaben	A2I8C7HI9T	IACT
Propylene Glycol	6DC9Q167V3	IACT
Propylparaben	Z8IX2SC1OH	IACT
ALCOHOL	3K9958V90M	IACT
Sodium Citrate	1Q73Q2JULR	IACT
Water	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
4f32e6df-2272-40ef-b2d6-08af71dd5a05			60e242bf-10e5-4627-a75d-b61c5302fbbb	2017-01-20	Warnings	Exact identifier spl id: 4f32e6df-2272-40ef-b2d6-08af71dd5a05 spl set id: 60e242bf-10e5-4627-a75d-b61c5302fbbb

Reported adverse events (FAERS/openFDA)#

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

Each Relief