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 |
|---|---|---|---|---|---|---|
| MAXIMUM STRENGTH Lidocaine Plus Menthol | LIDOCAINE, MENTHOL | ARMY AND AIR FORCE EXCHANGE SERVICE | 60f72061-d264-424e-b396-5a609076d352 | 2026-08-20 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 5980c527-6bcb-a846-e063-6294a90a0788 | 2026-08-20 | Warnings | M017 |
| Pain Relief Patches | CAMPHOR, MENTHOL, METHYL SALICYLATE | Amerisource Bergen | 5fb5e5ce-b268-4444-8b63-ea7ea6abf269 | 2026-08-20 | Warnings | M017 |
| Dr. Scholls Blister Pain Relief Complete Kit | LIDOCAINE | Scholl's Wellness Company LLC | 58c2b35c-e1ed-7ea8-e063-6294a90a1494 | 2026-08-19 | Warnings | M017 |
| Dr. Scholls Blister Pain Relief Complete Kit | LIDOCAINE | Scholl's Wellness Company LLC | 585e740b-e4fa-d2aa-e063-6294a90a0982 | 2026-08-19 | Warnings | M017 |
| Eagle Brand Muscular Balm | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 0822bcde-a8ad-be95-e063-6294a90ad208 | 2026-08-19 | Warnings | M017 |
| ANTI ITCH | HYDROCORTISONE | HyVee Inc | 1ab6bbb8-2b91-4c53-9168-b1e85ac296e9 | 2026-08-19 | Warnings | M017 |
| hydrocortisone 1 | HYDROCORTISONE | Kroger Company | f05edff2-2dc5-427c-b52c-518e0aaef4e0 | 2026-08-19 | Warnings | M017 |
| MedPride | HYDROCORTISONE | Shield Line LLC | 2f15d3b3-d1e6-4742-9eac-f956c0ffbba4 | 2026-08-18 | Warnings | M017 |
| Pain Relieving Cream Analgesic | MENTHOL, UNSPECIFIED FORM AND METHYL SALICYLATE | Garcoa, Inc. | 2f736307-5cd4-4a76-9044-4aeecba096cc | 2026-08-18 | Warnings | M017 |
| Lidocaine Pain Relief Roll on | PAIN RELIEF ROLL ON | NeilMed Pharmaceuticals Inc | 58ff9d2d-99e6-8f98-e063-6394a90a8de7 | 2026-08-17 | Warnings | M017 |
| Hydrocortisone with Aloe | HYDROCORTISONE CREAM 1/2% | Sun Pharmaceutical Industries, Inc. | 59337940-c9be-58af-e063-6394a90abe13 | 2026-08-16 | Warnings | M017 |
| SIERQ Numbing | MENTHOL | Putian Licheng District Zhijiancheng Trading Co., Ltd. | 5936c070-d8e4-56e8-e063-6294a90a5600 | 2026-08-16 | Warnings | M017 |
| Jakwork Numbing Cream | NUMBING CREAM | Guangzhou Jingliang Cosmetics Co., Ltd. | 5911d9b0-1acb-3546-e063-6294a90adb3a | 2026-08-15 | Warnings | M017 |
| Re-Lieved Lidocaine Patch | LIDOCAINE PATCH 4% | Transfer Technology | 59072f05-eefa-d823-e063-6394a90a0e1a | 2026-08-14 | Warnings | M017 |
| JJ Care First Aid Burn | BENZALKONIUM CHLORIDE, LIDOCAINE HCI | Nantong Health & Beyond Hygienic Products Inc. | c41621fb-c549-4394-a4cb-cb81ef8c98df | 2026-08-13 | Warnings | M017 |
| JJ Care | HYDROCORTISONE | Nantong Health & Beyond Hygienic Products Inc. | c88fa151-f8a8-4de2-98c9-71319bf53e36 | 2026-08-13 | Warnings | M017 |
| Hydrocortisone | HYDROCORTISONE | Safetec of America, Inc. | da2b3b2c-11e0-401b-bbd2-d019271d1b3d | 2026-08-13 | Warnings | M017 |
| CVS Pain Relief Roll-On Lidocaine with Lavender | LIDOCAINE HYDROCHLORIDE | CVS Pharmacy | 4aa53176-2103-b47b-e063-6394a90ac735 | 2026-08-12 | Warnings | M017 |
| JUST CBD SOOTHING | MENTHOL, CAMPHOR | Just Brands LLC | 5384e80f-c242-76a1-e063-6294a90aba0b | 2026-08-12 | 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 |