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 |
|---|---|---|---|---|---|---|
| EXOTEN-C | METHYL SALICYLATE, MENTHOL, CAPSAICIN | Asclemed USA, Inc. | 76ed37e0-64b5-4abe-a03c-3dc7084a3919 | 2023-10-16 | Warnings | M017 |
| Calypxo Pain Relief | METHYL SALICYLATE, MENTHOL | Asclemed USA, Inc | bd9d0bc0-5705-4c73-bcd6-f6cdb68e05b6 | 2023-10-16 | Warnings | M017 |
| Calypxo HP Pain Relief | METHYL SALICYLATE, MENTHOL | Asclemed USA, Inc | 89a8c267-bd92-4d0d-8e50-c52224aff9cd | 2023-10-16 | Warnings | M017 |
| Zylotrol | LIDOCAINE HCL 4%, MENTHOL 1% | Whitestone Products LLC | 0e32e9c0-ff5b-4e88-89b1-f5903cd98209 | 2023-10-16 | Warnings | M017 |
| Capsadyn | CAPSAICIN | Chorda Pharma, Inc | 07731045-0d2b-76b7-e063-6294a90af921 | 2023-10-11 | Warnings | M017 |
| WHITE FLOWER STRAIN RELIEF | CAMPHOR, MENTHOL AND METHYL SALICYLATE | HOE HIN PAK FAH YEOW MANUFACTORY LTD | 65282267-de63-453a-a686-f8752c71b9ef | 2023-10-02 | Warnings | M017 |
| WHITE FLOWER ANALGESIC BALM FLORAL SCENTED | CAMPHOR, MENTHOL AND METHYL SALICYLATE | HOE HIN PAK FAH YEOW MANUFACTORY LTD | 4e9cb5aa-b0aa-4a5c-b561-cc38437758d8 | 2023-10-02 | Warnings | M017 |
| NATUREANCE BODY BALM | CAMPHOR | EROS GLOBAL CORP | 05b84fd2-8d8f-9249-e063-6294a90ae29f | 2023-09-19 | Warnings | M017 |
| U ICE COLD | MENTHOL | UNIVERSAL DISTRIBUTION CENTER LLC | 752ef0cd-f12a-3b9e-e053-2991aa0abeb1 | 2023-09-01 | Warnings | M017 |
| Family Wellness Pain Relief with Lidocaine | PAIN RELIEF WITH LIDOCAINE | FAMILY DOLLAR (Family Wellness) | 3a18119f-6c75-4cea-a990-97cb8a9589d4 | 2023-08-29 | Warnings | M017 |
| Bactine Max Antibiotic and Lidocaine Max Pain Relief | LIDOCAINE | WellSpring Pharmaceutical Corporation | 71300df9-6113-4f25-93ca-28ad7e7f79de | 2023-06-08 | Warnings | M017 |
| Bactine Max Lidocaine Roll-on 2.5oz | LIDOCAINE | WellSpring Pharmaceutical Corporation | 09b32a98-9131-451e-87a6-81a1e4ed7ec5 | 2023-04-25 | Warnings | M017 |
| Icy Hot Pro Dry | CAMPHOR, MENTHOL | Chattem, Inc. | 4de1bc29-d166-4599-9e75-5f841bf20967 | 2023-03-01 | Warnings | M017 |
| Icy Hot Vanishing Scent | MENTHOL | Chattem, Inc. | e2092016-9741-433d-92e6-74bfddadb72c | 2022-09-29 | Warnings | M017 |
| New Terocin | METHYL SALICYLATE, CAPSAICIN, AND MENTHOL | Alexso, Inc | 5dbd5fc0-a27e-4979-aca7-28f73096fd5f | 2022-08-18 | Warnings | M017 |
| FIRSTAR Sting Relief Pad | BENZOCAINE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 0e491a7a-4204-439f-862d-741cbc0be9fd | 2021-07-06 | Warnings | M017 |
| Arthritis Relief GoodSense | TROLAMINE SALICYLATE | Geiss, Destin & Dunn, Inc | a253730a-2187-07de-e053-2a95a90a9877 | 2020-04-02 | Warnings | M017 |
| Aloe Cort | HYDROCORTISONE | Topiderm, Inc. | 789a6669-3320-4558-8d6f-ab255db50d8d | 2019-09-17 | Warnings | M017 |
| Eagle Brand Medicated Roll On Refresh | CAMPHOR, MENTHOL | Borden Company (Private) Limited | 567b6820-fb52-630e-e063-6294a90a8bf8 | 2015-07-01 | Warnings | M017 |
| Eagle Brand Medicated Oil Aromatic | CAMPHOR, MENTHOL, METHYL SALICYLATE | Borden Company (Private) Limited | 54e45d89-e8c3-6fc3-e063-6394a90aac4e | 2015-06-15 | 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 |