Itch Relief
- Product NDC
- 81522-751
- 11-digit product format
- 815220751
- Labeler code
- 81522
- Product ID
- 81522-751_4743491a-42d4-bf24-e063-6294a90a581c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- FSA Store Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-19
- 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 |
|---|---|
| 1050080 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 47434af6-0fdd-9615-e063-6394a90ab9e8 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 77dc03a4-fbfc-e6a3-fe95-285bbae40d75 | Product name | 2 | 20250814 |
| 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 |
|---|---|---|---|---|---|---|
| 81522-751-25 | Itch Relief | 74 mL in 1 BOTTLE, SPRAY | SPRAY | 74 | 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 |
|---|---|---|---|---|---|---|
| DO ME DELAY | LIDOCAINE HCL | Prodigy Media Inc | 5255ee85-6f29-0776-e063-6394a90a525b | 2026-05-21 | Warnings | M017 |
| Australian Dream Back Pain | HISTAMINE DIHYDROCHLORIDE | Sombra Cosmetics Inc. | 5256a63e-e6da-84c1-e063-6294a90a8dff | 2026-05-21 | Warnings | M017 |
| SINSIN HANBANG FLEX | CAMPHOR, MENTHOL | Sinsin Pharmaceutical co., ltd. | 525c5d18-bfc1-3002-e063-6394a90a5b1d | 2026-05-21 | Warnings | M017 |
| LidoPro Patch | LIDOCAINE, MENTHOL, AND METHYL SALICYLATE | Preferred Pharmaceuticals Inc. | 6c9a076e-6316-427b-9ce6-c8fe2d388837 | 2026-05-21 | Warnings | M017 |
| Medi-First Capsaicin Cream | CAPSAICIN | Unifirst First Aid Corporation | 49eb807b-fa31-3d84-e063-6394a90acfcf | 2026-05-20 | Warnings | M017 |
| Biofreeze Triple Target Roll-On | CAMPHOR, CAPSAICIN, MENTHOL | Reckitt Benckiser LLC | 5089c088-3026-233a-e063-6394a90a93b6 | 2026-05-19 | Warnings | M017 |
| Lidocaine Pain Relief Patch | LIDOCAINE | GERI-CARE PHARMACEUTICAL CORP | 522f1521-f9f2-4c26-e063-6394a90a9e05 | 2026-05-19 | Warnings | M017 |
| Easment 0.1% Capsaicin Roll on | CAPSAICIN 0.1% | Easment LLC | 521212d6-57fd-4a7a-e063-6294a90a2a18 | 2026-05-18 | Warnings | M017 |
| Burn Relief | LIDOCAINE | WALMART INC. | 15af4557-4baf-c177-e063-6294a90a7a5b | 2026-05-18 | Warnings | M017 |
| Blistex Maximum Hydration Lip | CAMPHOR (SYNTHETIC), DIMETHICONE, UNSPECIFIED, MENTHOL, UNSPECIFIED FORM, AND PHENOL | Blistex Inc. | fed223bc-edf3-46eb-b678-acb906f9ef11 | 2026-05-18 | Warnings | M017 |
| Tiger Balm | CAMPHOR (SYNTHETIC), MENTHOL, AND CAPSICUM | Haw Par Healthcare Ltd. | 5066dc10-e4d5-49e9-9a5f-0ac220cfbf28 | 2026-05-18 | Warnings | M017 |
| Deep Blue Mini | MENTHOL | doTERRA International, LLC | 51dd58a8-1fd5-9cd7-e063-6394a90a1f72 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Gel | MENTHOL | Reckitt Benckiser LLC | f5c8c08b-c7c0-f84d-e053-2a95a90add15 | 2026-05-15 | Warnings | M017 |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 00bba5d2-b0e0-701c-e063-6294a90a5741 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Roll-on | MENTHOL | Reckitt Benckiser LLC | f67d7b7a-8922-73f6-e053-2995a90a2e80 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Relief | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 07be6e88-1850-4d6a-946d-f03830b8c4a2 | 2026-05-15 | Warnings | M017 |
| Biofreeze Roll-On and Overnight Roll-On | MENTHOL | Reckitt Benckiser LLC | 4d3dcb8f-2075-6bbc-e063-6394a90a4992 | 2026-05-15 | Warnings | M017 |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 6bef9ccb-7a5a-4c67-b1bc-a92b167312da | 2026-05-15 | Warnings | M017 |
| Biofreeze Roll-On | MENTHOL | Reckitt Benckiser LLC | ebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb | 2026-05-15 | Warnings | M017 |
| Biofreeze Precision Relief Pen | MENTHOL | Reckitt Benckiser LLC | b4cc1db5-a33f-17bc-e053-2995a90ab7eb | 2026-05-15 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1050080 | diphenhydrAMINE HCl 2 % Topical Spray | PSN | 47434af6-0fdd-9615-e063-6394a90ab9e8 | 1 |
| 1050080 | diphenhydramine hydrochloride 20 MG/ML Topical Spray | SCD | 47434af6-0fdd-9615-e063-6394a90ab9e8 | 1 |
| 1050080 | diphenhydramine HCl 2 % Topical Spray | SY | 47434af6-0fdd-9615-e063-6394a90ab9e8 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 81522-751-25 | 81522075125 | 74 mL in 1 BOTTLE, SPRAY (81522-751-25) | 74 ml | 2025-08-19 | No | No | Current |