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 |
|---|---|---|---|---|---|---|
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35ac19-6883-a733-e063-6294a90ad22d | 2024-11-05 | Warnings | M017 |
| Alocane Plus | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products, Inc. | cfe8114b-df65-064b-e053-2a95a90a33f6 | 2024-11-05 | Warnings | M017 |
| Alocane Botanicals | LIDOCAINE HYDROCHLORIDE | Quest Products, LLC. | 02a8e5c7-56f4-eb0d-e063-6294a90a80cd | 2024-11-05 | Warnings | M017 |
| Alocane Emergency Burn Pads | LIDOCAINE HYDROCHLORIDE | Quest Products, Inc. | fe58bb89-7216-4121-afd3-d1438bdfbfa2 | 2024-11-05 | Warnings | M017 |
| Licefreee AfterLice | PRAMOXINE HCI | Tec Laboratories Inc. | 06c4cc42-a215-3949-e063-6394a90a665e | 2024-11-05 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | ASO LLC | cb9505b7-222d-3a24-e053-2a95a90a0b64 | 2024-11-05 | Warnings | M017 |
| TopCare Pain Relieving Analgesic | LIDOCAINE HYDROCHLORIDE | Topco Associates LLC | 6b4783e0-1987-4838-9e8c-b95426d62b28 | 2024-11-05 | Warnings | M017 |
| Eagle Green Balm | CAMPHOR MENTHOL | Borden Company (Private) Limited | 6f7a796b-a31c-0e60-e053-2a91aa0a022b | 2024-11-04 | Warnings | M017 |
| Muscular Balm | CAPSAICIN MENTHOL METHYL SALICYLATE | Borden Company (Private) Limited | ed79f14e-6b3d-4bf2-9c34-d019c1ba2582 | 2024-11-04 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE | A-S Medication Solutions | 3e0aed2b-fee1-4a0c-a3d2-72cd2b3008e3 | 2024-11-04 | Warnings | M017 |
| Walgreens Ice Blue Pain Relieving Topical Analgesic | MENTHOL, UNSPECIFIED FORM | Walgreen Company | 1c0ee442-ffd2-4f6c-aab2-f70e295378ad | 2024-11-04 | Warnings | M017 |
| Walgreen Cool n Heat Maximum Strength Pain Relieving | MENTHOL, UNSPECIFIED FORM | Walgreen Company | d5c79476-dde8-4a85-8878-bc2ac3a3d70b | 2024-11-04 | Warnings | M017 |
| LIDOCAINE | LIDOCAINE | STRATUS PHARMACEUTICALS INC | 87a4f559-a4f6-4b9f-98de-b55b073a11c6 | 2024-11-01 | Warnings | M017 |
| Walgreens Nerve Pain Relieving Topical Analgesic | LIDOCAINE HYDROCHLORIDE AND MENTHOL, UNSPECIFIED FORM | Walgreen Company | 83849eca-e02f-4b43-b3a7-b25e987e08a8 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica White | CAMPHOR | Sanvall Enterprises, Inc | 192039a2-aed6-821b-e063-6394a90a7f29 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Reforzada | CAMPHOR | Sanvall Enterprises, Inc | 1921a4b1-cd36-195e-e063-6294a90a8793 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Arnica Pain Releiving Roll On with Camphor | CAMPHOR | Sanvall Enterprises, Inc | 173db0e2-611f-55b9-e063-6394a90ac987 | 2024-10-31 | Warnings | M017 |
| Sanar Naturals Camphor | CAMPHOR | Sanvall Enterprises, Inc | 1921e851-cf83-0bdb-e063-6294a90a357f | 2024-10-31 | Warnings | M017 |
| cortisone | HYDROCORTISONE | CVS Pharmacy | c766deac-d993-4e48-a5c3-4cfde7338dff | 2024-10-31 | Warnings | M017 |
| Walgreens Pain Relieving with Lavender Analgesic | LIDOCAINE HYDROCHLORIDE | Walgreen Company | 6c7b39c8-5b65-430a-a529-5b6b14adce18 | 2024-10-31 | 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 |