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 |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 20 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| TC2D6JAD40 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1049880 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 44811828-c32e-17fc-e063-6294a90add48 | Available on FDA.report |
DailyMed Product Concepts#
| 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 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 13709-351-01 | Itch Relief | 1 in 1 CARTON | GEL | 1 | 1 | |
| 13709-351-01 | Itch Relief | 103.5 mL in 1 TUBE | GEL | 103.5 | 1 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Re-Lieved Lidocaine Patch | LIDOCAINE PATCH 4% | Transfer Technology | 37ef02d4-2ff5-cb23-e063-6294a90a68af | 2025-06-19 | Warnings | M017 |
| Post-Treatment Repair Cream | HYDROCORTISONE | Vi Medical Products Inc. | ab8885a9-0778-28ff-e053-2995a90a2e12 | 2025-06-19 | Warnings | M017 |
| MyDerm | LIDOCAINE | Inspec Solutions LLC. | 82d075d1-c92e-2097-e053-2991aa0ab131 | 2025-06-18 | Warnings | M017 |
| Walgreens Extra Small Lidocaine | LIDOCAINE | Walgreen Co. | dc838e47-d234-4ba5-9449-f645e99be923 | 2025-06-18 | Warnings | M017 |
| CLn Body Moisturizer | COLLOIDAL OAT MOISTURIZER | TopMD Skin Care, Inc. | 2de3d68d-a540-d456-e063-6394a90a4b57 | 2025-06-18 | Warnings | M017 |
| Aloe UP SPF 30 Mineral | ZINC OXIDE, TITANIUM DIOXIDE | Aloe Care International, LLC | 35967b33-bdfb-ee3c-e063-6294a90a75f6 | 2025-06-18 | Warnings | M017 |
| Aloe Up SPF 50 Mineral | ZINC OXIDE, TITANIUM DIOXIDE | Aloe Care International, LLC | 35b9dcfa-05f3-3d7b-e063-6394a90a18f1 | 2025-06-18 | Warnings | M017 |
| Aloe Up SPF 50 Mineral | ZINC OXIDE | Aloe International, LLC | 35bc3621-f4e4-42d3-e063-6394a90a7aad | 2025-06-18 | Warnings | M017 |
| Aloe Up SPF 50 Kids Mineral | ZINC OXIDE, TITANIUM DIOXIDE | Aloe Care International, LLC | 35cd16b0-bd81-8f68-e063-6294a90a3d8c | 2025-06-18 | Warnings | M017 |
| Aloe Up SPF 50 Kids Mineral | ZINC OXIDE | Aloe International, LLC | 35cd5542-947d-a042-e063-6394a90a13f8 | 2025-06-18 | Warnings | M017 |
| Relieve Your Pain | MENTHOL | Proximity Capital Partners LLC dba Asutra | c12369dd-8305-edaf-e053-2995a90a0d3d | 2025-06-18 | Warnings | M017 |
| Melt Pain Away | CAPSAICIN | Proximity Capital Partners LLC dba Asutra | a95a11d7-a2ae-6654-e053-2a95a90a802c | 2025-06-18 | Warnings | M017 |
| Recovery Roll-On | MENTHOL, CAMPHOR | PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA | ebc9630f-6d8b-e4f0-e053-2995a90a0b49 | 2025-06-18 | Warnings | M017 |
| ProCure Hydrocortisone 1% | HYDROCORTISONE | Twin Med LLC | 37cdfabc-1fdb-246a-e063-6394a90a008a | 2025-06-17 | Warnings | M017 |
| ProCure Hydrocortisone 1% | HYDROCORTISONE | Twin Med LLC | 37ce6c35-b211-43de-e063-6294a90ab773 | 2025-06-17 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE CREAM 1% | Sun Pharmaceutical Industries, Inc. | 312ddc8d-100e-cfac-e063-6294a90acd09 | 2025-06-16 | Warnings | M017 |
| Curist 5% Lidocaine | LIDOCAINE 5% | Little Pharma, Inc. | f20241a2-c5b1-f124-e053-2995a90a891b | 2025-06-16 | Warnings | M017 |
| Toast Screamin Menthol | MENTHOL | IDEAZ, LLC | 37b48b1a-ef3d-afdc-e063-6294a90a6610 | 2025-06-16 | Warnings | M017 |
| Toast Freezin Cold | MENTHOL, METHYL SALICYLATE | IDEAZ, LLC | 37b4d363-0099-8cd3-e063-6394a90a18d6 | 2025-06-16 | Warnings | M017 |
| Earths Care Anti-Itch | CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM | DLC Laboratories, Inc. | ba65f58a-d590-498a-b8e7-a3d78935d880 | 2025-06-13 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049880 | diphenhydrAMINE HCl 2 % Topical Gel | PSN | 44811828-c32e-17fc-e063-6294a90add48 | 1 |
| 1049880 | diphenhydramine hydrochloride 0.02 MG/MG Topical Gel | SCD | 44811828-c32e-17fc-e063-6294a90add48 | 1 |
| 1049880 | diphenhydramine hydrochloride 2 % Topical Gel | SY | 44811828-c32e-17fc-e063-6294a90add48 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 13709-351-01 | 13709035101 | 1 TUBE in 1 CARTON (13709-351-01) / 103.5 mL in 1 TUBE | 1 tube | 2025-11-26 | No | No | Current |