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 |
|---|---|---|---|---|---|---|
| Lidocaine 4% Topical Anesthetic Cream | LIDOCAINE 4% | Oncor Pharmaceuticals | 1baaa669-05af-4024-a0ba-ee3451756f6a | 2026-01-05 | Warnings | M017 |
| TheraCare Pain Relief | MENTHOL | Veridian Healthcare | 6834a6de-4d1d-4e40-945d-ec5c267abd14 | 2026-01-05 | Warnings | M017 |
| TheraCare Lidocaine Pain Relief | LIDOCAINE | Veridian Healthcare | ee8cd550-64ee-432e-98e5-b68083179a3c | 2026-01-05 | Warnings | M017 |
| REGENECARE HA | LIDOCAINE HCL | MPM Medical LLC | 0eee554f-dfe0-433a-9665-8bdb95229888 | 2026-01-05 | Warnings | M017 |
| Pain Relieving Cream | CAMPHOR AND MENTHOL | PAIN WIZARD LIMITED LIABILITY COMPANY | 2647bba1-87f4-3c16-e063-6394a90ae0c9 | 2026-01-05 | Warnings | M017 |
| TheraCare Lidocaine plus Menthol | LIDOCAINE, MENTHOL | Veridian Healthcare | efddd116-d753-425a-9ded-09b8045024e4 | 2026-01-05 | Warnings | M017 |
| TheraCare Original Menthol | MENTHOL | Veridian Healthcare | ea56e4e1-a758-428b-8758-ee31bb00ca82 | 2026-01-05 | Warnings | M017 |
| Mugwort Patch (Cervical spine use) | 2%MENTHOL | YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED | 478e220c-0d35-9ee0-e063-6294a90ab689 | 2026-01-04 | Warnings | M017 |
| Mugwort Patch (Lumbar spine use) | 2%MENTHOL | YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED | 478e4b21-6d81-4cd3-e063-6394a90a18fe | 2026-01-04 | Warnings | M017 |
| Mugwort Patch (Knee use) | 2%MENTHOL | YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED | 478e86d2-3030-91eb-e063-6394a90a4db0 | 2026-01-04 | Warnings | M017 |
| American Safety and First Aid | HYDROCORTISONE ACETATE | Orazen Inc | 4a543f90-d43c-4487-b27e-f43394c6320d | 2026-01-04 | Warnings | M017 |
| Doctor Hoys Pain Relief Gel | MENTHOL, CAMPHOR (SYNTHETIC) | Dynamic Blending Specialists, Inc. | 50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8 | 2026-01-02 | Warnings | M017 |
| Doctor Hoys Pain Relief Gel Roll-On | MENTHOL, CAMPHOR (SYNTHETIC) | Dynamic Blending Specialists, Inc. | bf47acb2-6c90-4d5c-820b-447cac9305a4 | 2026-01-02 | Warnings | M017 |
| Amino Rip Muscle Pain Relief | LIDOCAINE HCL | LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION | 2bed5764-4217-4aa3-9d90-3b5460dcffa3 | 2026-01-02 | Warnings | M017 |
| Menthozen Cream | METHYL SALICYLATE, MENTHOL, CAPSAICIN | Village Pharma LLC | 63bb0283-cfbe-4e9c-8772-73062c0c8d05 | 2026-01-01 | Warnings | M017 |
| Menthozen Hydrogel | MENTHOL, CAPSAICIN | Village Pharma LLC | 4c979a71-7c8f-4dff-abae-bf4cdf8f67b4 | 2026-01-01 | Warnings | M017 |
| Lidozen Gel | LIDOCAINE HYDROCHLORIDE, MENTHOL | Village Pharma LLC | ffb7831f-4ca9-4d73-8303-e9cd90078982 | 2026-01-01 | Warnings | M017 |
| Sting Relief | BENZOCAINE, ISOPROPYL ALCOHOL | Yiwu Ori-Power Medtech Co.,Ltd. | 116ee6dc-9c49-2e11-e063-6394a90a44ed | 2026-01-01 | Warnings | M017 |
| Menthozen | METHYL SALICYLATE, MENTHOL, CAPSAICIN | Village Pharma LLC | 48b1b99e-d0ec-4e5c-b80c-c0d2d87ecb13 | 2026-01-01 | Warnings | M017 |
| NUVALU ICE THERAPY MENTHOL PAIN RELIEVING | MENTHOL | JC SALES | 5adf457e-b4d0-30c8-e063-6294a90a64b9 | 2026-01-01 | 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 |