After Bite Xtra
- Product NDC
- 44224-1276
- 11-digit product format
- 442241276
- Labeler code
- 44224
- Product ID
- 44224-1276_5ccc1abc-d46b-94ca-e063-6394a90a185f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Tender Corporation d/b/a Adventure Ready Brands
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-01
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- .4 g/20g
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- After Bite Xtra
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | .4 g/20g |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 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 |
|---|---|---|---|---|---|---|
| 44224-1276-0 | After Bite Xtra | 1 g in 1 TUBE | GEL | 1 | 2 | |
| 44224-1276-1 | After Bite Xtra | 1 in 1 BOX | GEL | 1 | 2 |
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 |
|---|---|---|---|---|---|---|
| After Bite Outdoor | DIPHENHYDRAMINE HCL | Tender Corporation d/b/a Adventure Ready Brands | 22b891a9-6386-dee1-e063-6394a90a5c2f | 2025-11-14 | Warnings | M017 |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 8f8f53e3-fe31-e7b5-e053-2995a90a710d | 2025-11-14 | Warnings | M017 |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 9984a510-30be-4013-e053-2995a90a841e | 2025-11-14 | Warnings | M017 |
| Anti-Itch Cream | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE | Kroger | 3f881349-fcdd-e276-e063-6394a90ae49e | 2025-11-13 | Warnings | M017 |
| Rapid Relief | PLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 434cb8b2-a996-5360-e063-6394a90ada03 | 2025-11-13 | Warnings | M017 |
| Rapid Relief | COLD RELIEF PATCH 5% MENTHOL | RAPID AID VIET NAM COMPANY LIMITED | 4360e3ec-7a4b-b28e-e063-6294a90a0bd6 | 2025-11-13 | Warnings | M017 |
| Rapid Relief | PAIN RELIEF PATCH CAMPHOR 110MG MENTHOL 33MG CAPSICUM EXTRACT 22MG | RAPID AID VIET NAM COMPANY LIMITED | 4360e3be-0ec4-cd57-e063-6394a90aca63 | 2025-11-13 | Warnings | M017 |
| Rapid Relief | PAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 43616ad7-58bb-e5ad-e063-6394a90a192b | 2025-11-13 | Warnings | M017 |
| 4x Medicated Severe Toothache and Gum Gel | BENZALKONIUM CHLORIDE | Meijer | 97ce7890-5093-1763-e053-2a95a90afae7 | 2025-11-13 | Warnings | M017 |
| Pain Reliever | CAMPHOR, MENTHOL | Kool 'N Fit Inc. | 2253f6bd-5707-b993-e063-6394a90aa74a | 2025-11-13 | Warnings | M017 |
| Rapid Relief | PLANTAR FASCIITIS PAIN RELIEF LIDOCAINE 4% MENTHOL 1% | RAPID AID VIET NAM COMPANY LIMITED | 4360e0d1-46cd-ab4b-e063-6394a90a55e1 | 2025-11-12 | Warnings | M017 |
| CVS Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | CVS | 8723e097-296f-784a-e053-2991aa0a552e | 2025-11-12 | Warnings | M017 |
| Dragon Pain Relieving Balm | CAMPHOR, MENTHOL | Americanna Wellness, Inc. | 154d8821-3e76-b0e2-e063-6294a90ae077 | 2025-11-12 | Warnings | M017 |
| Good neighbor Pharmacy Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | AMERISOURCEBERGEN DRUG CORPORATION | 87395273-380c-7cef-e053-2991aa0a54c6 | 2025-11-12 | Warnings | M017 |
| Quality Choice Itch Relief | DIPHENHYDRAMINE HCL, ZINC ACETATE | Chain Drug Marketing Association | 8735b298-83f3-0b5d-e053-2a91aa0a8292 | 2025-11-12 | Warnings | M017 |
| Dragon Pain Relieving Balm | CAMPHOR, MENTHOL | Americanna Wellness, Inc. | 1550e794-b3c0-4769-e063-6294a90a8c2d | 2025-11-12 | Warnings | M017 |
| Dragon Pain Relieving Balm | CAMPHOR, MENTHOL | Americanna Wellness, Inc. | 154fd46e-f00d-1772-e063-6394a90aba7d | 2025-11-12 | Warnings | M017 |
| Best Choice Itch Stopping | DIPHENHYDRAMINE HCL | Valu Merchandisers | 884cfd64-2cd1-8c12-e053-2995a90a8925 | 2025-11-12 | Warnings | M017 |
| Itch Stopping | DIPHENHYDRAMINE HCL | CVS | 8839149d-e6d5-57cc-e053-2995a90a9832 | 2025-11-12 | Warnings | M017 |
| Itch Stopping | DIPHENHYDRAMINE HCL | Chain Drug Marketing Association | 884c9b47-d511-1d17-e053-2995a90a42eb | 2025-11-12 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1049880 | diphenhydrAMINE HCl 2 % Topical Gel | PSN | 22b8b83e-66d6-0caa-e063-6394a90ad6fd | 2 |
| 1049880 | diphenhydramine hydrochloride 0.02 MG/MG Topical Gel | SCD | 22b8b83e-66d6-0caa-e063-6394a90ad6fd | 2 |
| 1049880 | diphenhydramine hydrochloride 2 % Topical Gel | SY | 22b8b83e-66d6-0caa-e063-6394a90ad6fd | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 44224-1276-0 | 44224127600 | 1 g in 1 TUBE | 1 g | Historical | |||
| 44224-1276-1 | 44224127601 | 1 TUBE in 1 BOX (44224-1276-1) / 1 g in 1 TUBE (44224-1276-0) | 1 tube | 2025-01-01 | No | No | Current |