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 |
|---|---|---|---|---|---|---|
| SunBurnt PLUS | LIDOCAINE HYDROCHLORIDE | Quest Products, LLC. | 12128c75-015d-8a72-e063-6394a90ae00a | 2024-02-23 | Warnings | M017 |
| Kroger Analgesic Analgesic | LIDOCAINE HYDROCHLORIDE | THE KROGER CO | e6c5ead3-87d0-48ed-a4dc-86cf89ebb285 | 2024-02-22 | Warnings | M017 |
| Rugby Pain Relieving Analgesic | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Bryant Ranch Prepack | fcf48536-224e-4a3d-9124-770031823972 | 2024-02-22 | Warnings | M017 |
| meijer ROLL-ON Cold Therapy Pain Relieving Topical analgesic | MENTHOL, UNSPECIFIED FORM | Meijer Distribution, Inc | 8bc3956b-b82d-4ed3-8bc3-db0078466bbc | 2024-02-22 | Warnings | M017 |
| Promescent Delay Wipes | BENZOCAINE | Absorption | f0a5b6be-acc5-473c-9054-b9534e769db1 | 2024-02-20 | Warnings | M017 |
| Ralli Rapid Pain Relief | MENTHOL | Troy Manufacturing, Inc. | 721658dc-3b1d-43ff-9032-e96851633cf9 | 2024-02-19 | Warnings | M017 |
| Ralli Rapid Pain Relief Roll on | MENTHOL | Troy Manufacturing, Inc. | 978d5c2c-fdc4-4d25-83ec-0b9404ec8018 | 2024-02-19 | Warnings | M017 |
| 1168 | 1168 BURN SPRAY | Dynarex Corporation | 1183a4f5-f875-dfb0-e063-6394a90af35f | 2024-02-16 | Warnings | M017 |
| Pain Relief | BENZOCAINE | Safetec of America, Inc. | de84e598-d047-4fae-b2ed-155a3788bc6f | 2024-02-16 | Warnings | M017 |
| No Mess Hydrocortisone Applicator | HYDROCORTISONE | Walgreen Co. | cfefb517-9099-41c4-8a95-74414ca4032c | 2024-02-16 | Warnings | M017 |
| Analgesic Balm | MENTHOL 10%, METHYL SALICYLATE 15% | Geri-Care Pharmaceuticals, Corp | ab9bf09d-bc8c-6d17-e053-2995a90a6c36 | 2024-02-14 | Warnings | M017 |
| Natures Oil 16% Menthol | MENTHOL, UNSPECIFIED FORM | NATURAL ESSENTIALS, INC. | 2fbe23b7-23a3-4f0b-bc08-0205256f5d68 | 2024-02-14 | Warnings | M017 |
| Rugby Pain Relieving Analgesic | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Rugby Laboratories | 4c11876c-57ec-4429-a8c4-fb95baa4074a | 2024-02-13 | Warnings | M017 |
| Itch stopping Cream | DIPHENHYDRAMINE HYDROCHLORIDE 2%, ZINC ACETATE 0.1% | Trifecta Pharmaceuticals USA, LLC. | 11368823-d4af-a536-e063-6294a90a7a2e | 2024-02-12 | Warnings | M017 |
| Walgreens Boil Pain Relief | BOIL PAIN RELIEF | Walgreens Company | d11bd769-68d0-4057-bc2a-72719f16011e | 2024-02-12 | Warnings | M017 |
| Capsaicin | CAPSAICIN | Rugby Laboratories | c5915c84-84a2-46f6-9f97-0d9873e9944a | 2024-02-12 | Warnings | M017 |
| Leader Ice Blue Analgesic | MENTHOL, UNSPECIFIED FORM | Cardinal Health, 110 dba LEADER | 952e56ea-5cbc-4078-bd01-5d3b6864a5ce | 2024-02-09 | Warnings | M017 |
| Leader Ultra Strength Muscle Rub Topical Analgesic | CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE | Cardinal Health, 110 dba LEADER | 9d99a900-60e0-454c-98e0-2c63eb910cf1 | 2024-02-09 | Warnings | M017 |
| Pain Relieving | CAMPHOR (NATURAL) | J.R. Watkins, LLC. | 28821ffa-a138-47b5-8857-beadf7a20d43 | 2024-02-08 | Warnings | M017 |
| Menthol Camphor Cough Suppressant Topical Analgesic Rub | CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM | J.R. Watkins, LLC. | fd0ea70a-ef12-48b1-8d9d-cc5f6417f854 | 2024-02-08 | 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 |