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 |
|---|---|---|---|---|---|---|
| Nufabrx Medicine Infused Socks | CAPSAICIN | Nufabrx LLC | 00d7d5bf-ee03-e73d-e063-6394a90a5d94 | 2025-10-15 | Warnings | M017 |
| Nufabrx Medicine Infused Elbow Sleeve | CAPSAICIN | Nufabrx LLC | 27ef3ef0-2f98-6672-e063-6294a90aeca4 | 2025-10-15 | Warnings | M017 |
| Nufabrx Medicine Infused Wrist Sleeve | CAPSAICIN | Nufabrx LLC | 22572cf9-fc0c-d327-e063-6394a90a2186 | 2025-10-15 | Warnings | M017 |
| Antibacterial Lidocaine Wound Gel | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | WALGREENS | eff77965-dc7f-49af-e053-2995a90a1a97 | 2025-10-14 | Warnings | M017 |
| Pleasure Balm Kama Sutra | BENZOCAINE | Cosmetic Enterprises Ltd | f370e3c4-65ca-4f3c-a5aa-70e198e681a2 | 2025-10-14 | Warnings | M017 |
| Vanicream HC Anti-Itch | HYDROCORTISONE | Pharmaceutical Specialties, Inc. | 28b06507-27a5-2cb1-e054-00144ff8d46c | 2025-10-14 | Warnings | M017 |
| Trilogel | LIDOCAINE HYDROCHLORIDE | Trifluent Pharma LLC | 22af7d63-6a56-4a38-a95b-0f88410b23cb | 2025-10-14 | Warnings | M017 |
| PROINNATE Numbing Cream | MENTHOL | Guangzhou Haishi Biological Technology Co., Ltd. | 40c63645-8ed3-82b3-e063-6294a90a5267 | 2025-10-13 | Warnings | M017 |
| Cramergesic | MENTHOL, METHYL SALICYLATE | The Hygenic Company, LLC | d0ffde7a-6942-74fc-e053-2a95a90a484a | 2025-10-13 | Warnings | M017 |
| Tricylate | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Trifluent Pharma LLC | 4869b63a-e01e-4a79-a493-7a1b4d3e914b | 2025-10-13 | Warnings | M017 |
| Doloflex Pain Relief | MENTHOL, METHYL SALICYLATE | United Health & Beauty Corp | 32a830cc-04d3-102e-e063-6294a90a1cad | 2025-10-12 | Warnings | M017 |
| Lidocaine Pain Relieving Gel-Patch | LIDOCAINE | Nanjing Anxing Medical Technology Co., Ltd. | 40c9b132-57ce-865e-e063-6394a90a2080 | 2025-10-10 | Warnings | M017 |
| Kinesys | ZINC OXIDE | Wilc Healthcare Inc | a32b44c3-eda0-48ea-95fc-250a2c2396ca | 2025-10-10 | Warnings | M017 |
| Te-Fu Recovery Massage | MENTHOL, METHYL SALICYLATE | Wasatch Product Development | 7bc2989f-dfb6-e8af-e053-2991aa0a0bf2 | 2025-10-10 | Warnings | M017 |
| Anti-itch | HYDROCORTISONE | Medline Industries, LP | b0947381-c0db-4253-ab40-3d45603ae65d | 2025-10-09 | Warnings | M017 |
| Kalaya Pain Relief | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | e2452c4b-2548-497f-828b-5d960402522a | 2025-10-08 | Warnings | M017 |
| Kalaya Pain Relief 6X with Arnica | PAIN RELIEF CREAM | Avaria Health & Beauty Corp | 60198d2e-4de3-3fa0-e053-2a91aa0afaf7 | 2025-10-08 | Warnings | M017 |
| KALAYA PAIN RELIEF 6X WITH ARNICA - Pain Relief | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | 9b9b7cad-a5e2-4445-856b-4aa439d77a80 | 2025-10-08 | Warnings | M017 |
| KALAYA FOAMING PAIN RELIEF | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | d5021e6d-f29f-446b-874c-bdcabd9cf4f6 | 2025-10-08 | Warnings | M017 |
| KALAYA EXTRA STRENGTH FOAMING PAIN RELIEF | METHYL SALICYLATE, MENTHOL, CAMPHOR | Avaria Health & Beauty Corp | e0c9f22a-165a-4558-ba3c-8592f1bd0016 | 2025-10-08 | 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 |