Benadryl Extra Strength Itch Relief
- Product NDC
- 69968-0459
- 11-digit product format
- 699680459
- Labeler code
- 69968
- Product ID
- 69968-0459_399004db-8df3-c030-e063-6294a90a260b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Kenvue Brands LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-06-01
- Substance
- ZINC ACETATE; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 1; 20 mg/mL; mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], 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
- Benadryl Extra Strength Itch Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ZINC ACETATE | 1 mg/mL |
| DIPHENHYDRAMINE HYDROCHLORIDE | 20 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| FM5526K07A | Internal UNII lookup |
| TC2D6JAD40 | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 309d9be0-e367-429a-a1fa-ab7855477c8a | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 77dc03a4-fbfc-e6a3-fe95-285bbae40d75 | Product name | 2 | 20250814 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 0e2e0f88-b076-afe1-4bdd-32bca4375bec | Product name | 3 | 20250127 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
| 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 |
|---|---|---|---|---|---|---|
| 69968-0459-1 | Benadryl Extra Strength Itch Relief | 1 in 1 CARTON | SOLUTION | 1 | 8 | |
| 69968-0459-1 | Benadryl Extra Strength Itch Relief | 14 mL in 1 APPLICATOR | SOLUTION | 14 | 8 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69968-0459-1 | ML - Milliliter | 69968-0459 | 9fdb0baa-a35e-4a36-8cfc-37a065d225af | 1 | 2022-06-06 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0459 | BENADRYL EXTRA STRENGTH ITCH RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE) SOLUTION [KENVUE BRANDS LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241103_309d9be0-e367-429a-a1fa-ab7855477c8a.zip |
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 |
|---|---|---|---|---|---|---|
| 4x Medicated Toothache and Gum Cream | BENZOCAINE | Kroger | a8c5090a-24f9-4e73-e053-2a95a90acca0 | 2025-11-14 | Warnings | M017 |
| PM Toothache Relief | BENZOCAINE | CVS | 0a5a8cd0-d680-8a0f-e063-6294a90aa65c | 2025-11-14 | Warnings | M017 |
| PM Toothache Relief | BENZOCAINE | Walgreens | e816f742-fba9-3c12-e053-2a95a90a192f | 2025-11-14 | Warnings | M017 |
| 4x Medicated Toothache and Gum Cream | BENZOCAINE | Walgreens | a71c2092-4ece-b82e-e053-2995a90ac933 | 2025-11-14 | Warnings | M017 |
| 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 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1294591 | Benadryl 2 % / 0.1 % Topical Solution | PSN | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294589 | diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Solution | PSN | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294591 | diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution [Benadryl Itch Stopping] | SBD | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294589 | diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution | SCD | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294591 | Benadryl Extra Strength (diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % ) Topical Solution | SY | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294591 | Benadryl Extra Strength Itch Relief Stick (diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % ) Topical Solution | SY | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
| 1294589 | diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Solution | SY | 309d9be0-e367-429a-a1fa-ab7855477c8a | 8 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69968-0459-1 | 69968045901 | 1 APPLICATOR in 1 CARTON (69968-0459-1) / 14 mL in 1 APPLICATOR | 1 applicator | 2019-06-01 | 0000-00-00 | No | No | Current |