Itch Relief

Product NDC
13709-351
11-digit product format
137090351
Labeler code
13709
Product ID
13709-351_44811828-c32f-17fc-e063-6294a90add48
Type
HUMAN OTC DRUG
Nonproprietary name
Itch Relief Gel
Dosage form
GEL
Route
TOPICAL
Labeler
Neilmed Pharmaceuticals Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-11-26
Substance
DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
20 mg/mL
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Itch Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DIPHENHYDRAMINE HYDROCHLORIDE20 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
TC2D6JAD40Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1049880Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
44811828-c32e-17fc-e063-6294a90add48Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13709-351-01Itch Relief1 in 1 CARTONGEL11
13709-351-01Itch Relief103.5 mL in 1 TUBEGEL103.51

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 111 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pain Relief PatchesCAMPHOR, MENTHOL, METHYL SALICYLATEWalgreen Companydb8cf218-7544-4871-b1c3-a50a3d3e59f12024-12-17WarningsExact identifier
application number: M017
Albertsons Pain Relief PatchLIDOCAINESafewaydc2823bb-8586-daca-e053-2995a90a2af02024-12-17WarningsExact identifier
application number: M017
CAPSAICIN HEAT PATCHES BACK AND LARGE AREASCAPSAICINWalgreen Companye77167ab-6cb8-4d5b-838c-b0acc05e38892024-12-17WarningsExact identifier
application number: M017
Hot and Cold Medicated PatchMENTHOLWalgreen Companyd9fc133d-ebaa-48f1-a6f9-62453970012b2024-12-17WarningsExact identifier
application number: M017
PAIN RELIEF PATCHESLIDOCAINEWalgreen Company204b96bc-af4e-4842-8b57-7b416feb4dd92024-12-17WarningsExact identifier
application number: M017
Lidocaine DryLIDOCAINECVSbb7955fe-5113-1662-e053-2a95a90a85a12024-12-16WarningsExact identifier
application number: M017
HealthWise Medicated Original Body Powder 10 ozMENTHOLVeridian Healthcare296b623a-14cd-0bca-e063-6394a90ac5ff2024-12-16WarningsExact identifier
application number: M017
HealthWise Medicated Extra Body Powder 10 ozMENTHOLVeridian Healthcare296c9a9c-e3db-59fe-e063-6294a90a0b622024-12-16WarningsExact identifier
application number: M017
Rite Aid Hot and Cold Roll OnMENTHOL 16%Rite Aidfc4b2635-280b-267f-e053-6294a90a5e222024-12-15WarningsExact identifier
application number: M017
Rite Aid Pain RelievingBENZOCAINE 20%, MENTHOL 0.5%Rite Aide2c09e85-be0a-4e6d-e053-2995a90ad7562024-12-15WarningsExact identifier
application number: M017
Rugby LidocaineLIDOCAINE 4%Rugby Laboratoriesd94292f7-10fc-48bf-e053-2995a90a84722024-12-15WarningsExact identifier
application number: M017
Rite Aid CortisoneHYDROCORTISONE 1%Rite Aide27353b9-23b6-3801-e053-2a95a90a60452024-12-15WarningsExact identifier
application number: M017
Rite Aid Cooling Pain ReliefMENTHOL 10.5%Rite Aide2225259-70ec-52de-e053-2a95a90a73f82024-12-15WarningsExact identifier
application number: M017
Rite Aid Rectal CareLIDOCAINE 5%Rite Aide283e462-96e8-04cf-e053-2a95a90a1d002024-12-15WarningsExact identifier
application number: M017
Rite Aid Anti-ItchDIPHENHYDRAMINE HCL 2%Rite Aide33898d8-1b8b-5c0b-e053-2995a90add082024-12-15WarningsExact identifier
application number: M017
Rite Aid Cala Itch ReliefPRAMOXINE HCL 1%, ZINC ACETATE 0.1%Rite Aide29a9d59-4c7c-81aa-e053-2995a90a70562024-12-15WarningsExact identifier
application number: M017
CVS Roll-OnCAPSAISIN 0.1%CVSe8812c49-335e-61ea-e053-2995a90a17aa2024-12-15WarningsExact identifier
application number: M017
Good Sense Burn Relief AloeLIDOCAINE HCLGeiss, Destin & Dunn, Incb5a7f629-a88d-b49d-e053-2995a90a49fa2024-12-15WarningsExact identifier
application number: M017
QC Burn Relief AloeLIDOCAINE HCLChain Drug Marketing Association Incb5e76f0c-0bfe-b13e-e053-2995a90a08612024-12-15WarningsExact identifier
application number: M017
Meijer Burn ReliefLIDOCAINE 0.5%Meijerbec60c93-5abd-ee04-e053-2a95a90acb612024-12-15WarningsExact identifier
application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049880diphenhydrAMINE HCl 2 % Topical GelPSN44811828-c32e-17fc-e063-6294a90add481
1049880diphenhydramine hydrochloride 0.02 MG/MG Topical GelSCD44811828-c32e-17fc-e063-6294a90add481
1049880diphenhydramine hydrochloride 2 % Topical GelSY44811828-c32e-17fc-e063-6294a90add481

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
13709-351-01137090351011 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE1 tube2025-11-26NoNoCurrent