Xpect Extra Strength Itch Relief
- Product NDC
- 42961-218
- 11-digit product format
- 429610218
- Labeler code
- 42961
- Product ID
- 42961-218_43b08582-e9bb-4ba4-a2ca-7eab3c9c16c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Cintas Corporation
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-05-16
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 2 mg/100mL
- 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
- Xpect Extra Strength Itch Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 2 mg/100mL |
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 |
|---|---|
| a373b2c3-5c58-4b64-9358-bdf42dfce08c | 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 |
|---|---|---|---|---|---|---|
| 42961-218-01 | Xpect Extra Strength Itch Relief | 59.1 mL in 1 BOTTLE, SPRAY | SPRAY | 59.1 | 4 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Aromalief Pain Relief Cream Orange Ginger | MENTHOL | Marketites LLC | 9e8d3611-ef1b-4ac6-e053-2995a90af28a | 2025-10-29 | Warnings | M017 |
| Aromalief Calming Pain Relief Cream Lavender | MENTHOL | Marketites LLC | b8197d52-ccfb-b008-e053-2995a90a0a53 | 2025-10-29 | Warnings | M017 |
| Aromalief Cozy Vanilla Pain Relief Cream | MENTHOL | Marketites LLC | 3634e55e-8c62-a782-e063-6394a90a6508 | 2025-10-29 | Warnings | M017 |
| BENOVA PAIN AND ITCH RELIEF | MENTHOL, 0.11% | BENOVA RX LLC | 42513ee2-8b40-a9f3-e063-6394a90a9386 | 2025-10-29 | Warnings | M017 |
| Burn Relief | LIDOCAINE | CVS Pharmacy | 7e9285fd-26d5-3eac-e053-2991aa0ae2db | 2025-10-29 | Warnings | M017 |
| Coralite Ultra Strength Pain Relief | CAMPHOR MENTHOL | United Exchange Corp. | 44ecf959-cc07-4adc-a500-075b2ee69548 | 2025-10-29 | Warnings | M017 |
| GoodSense Pain Relief | LIDOCAINE | Geiss, Destin & Dunn, Inc | 826f8da4-8468-ea0a-e053-2991aa0a66cb | 2025-10-28 | Warnings | M017 |
| CALMADOL | CAMPHOR, MENTHOL, METHYL SALICYLATE | GRANDALL DISTRIBUTING, LLC | 31b7f84e-8b66-4d31-8e9c-279d0af2fe64 | 2025-10-28 | Warnings | M017 |
| XRay DOL | CAMPHOR, MENTHOL, AND METHYL SALICYLATE | Genomma Lab USA, Inc. | e07fef46-68d9-769c-e053-2a95a90aa065 | 2025-10-28 | Warnings | M017 |
| CVS Medicated Heat | CAPSICUM EXTRACT | CVS Pharmacy | 81cd1019-93a6-311b-e053-2991aa0a7997 | 2025-10-28 | Warnings | M017 |
| Foster and Thrive | LIDOCAINE | STRATEGIC SOURCING SERVICES, LLC | f950b072-d978-b629-e053-6394a90abfaf | 2025-10-28 | Warnings | M017 |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Premier Brands of America, Inc. | d3452573-f91f-f157-e053-2a95a90a1ad8 | 2025-10-27 | Warnings | M017 |
| PR | MENTHOL | Amphp, Inc | 6f5b9e08-c445-4fac-e053-2a91aa0aa737 | 2025-10-27 | Warnings | M017 |
| Lidocaine | BURN RELIEF | Foodhold USA | b25dc0df-02d0-41ac-b36c-2c04baa77ef2 | 2025-10-27 | Warnings | M017 |
| Menthol | MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE | FSA Store Inc. | fb3548c8-f202-dc50-e053-6394a90a5b30 | 2025-10-27 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE CONTINUOUS SPRAY | Premier Brands of America, Inc. | d344f68b-9b62-3029-e053-2995a90a1665 | 2025-10-27 | Warnings | M017 |
| Medi-First Hydrocortisone 1% | HYDROCORTISONE ACETATE 1% | Unifirst First Aid Corporation | f2b46d69-1c21-5ae9-e053-2a95a90a60a9 | 2025-10-24 | Warnings | M017 |
| Extra Strength | MENTHOL AND METHYL SALICYLATE | Saje Natural Business Inc. | 87d872b3-3231-d0f2-e053-2995a90a9d98 | 2025-10-24 | Warnings | M017 |
| Coralite Muscle and Joint Pain Relief | CAMPHOR, MENTHOL, AND MEHTYL SALICYLATE | United Exchange Corporation | 78edeeb8-3e3c-64bb-e053-2a91aa0a7bbc | 2025-10-24 | Warnings | M017 |
| Coralite Odor Free Pain Relief | LIDOCAINE | United Exchange Corporation | 7966d9f2-22f9-a900-e053-2991aa0aba55 | 2025-10-24 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1050080 | diphenhydrAMINE HCl 2 % Topical Spray | PSN | a373b2c3-5c58-4b64-9358-bdf42dfce08c | 4 |
| 1050080 | diphenhydramine hydrochloride 20 MG/ML Topical Spray | SCD | a373b2c3-5c58-4b64-9358-bdf42dfce08c | 4 |
| 1050080 | diphenhydramine HCl 2 % Topical Spray | SY | a373b2c3-5c58-4b64-9358-bdf42dfce08c | 4 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 42961-218-01 | 42961021801 | 59.1 mL in 1 BOTTLE, SPRAY (42961-218-01) | 59.1 ml | 2022-05-16 | 0000-00-00 | No | No | Current |