Diphenhydramine HCl and Zinc Acetate
- Product NDC
- 41250-058
- 11-digit product format
- 412500058
- Labeler code
- 41250
- Product ID
- 41250-058_2479e274-3585-44d6-e063-6394a90a7810
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Extra Strength Itch Relief
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-09-15
- Marketing end
- 2027-05-31
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
- Active strength
- 1.52; .076 g/76g; g/76g
- 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
- 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
- Diphenhydramine HCl and Zinc Acetate
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 1.52 g/76g |
| ZINC ACETATE | .076 g/76g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| TC2D6JAD40 | Internal UNII lookup |
| FM5526K07A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1053138 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 18998e1c-1254-4d0c-93f1-26652c5ca076 | 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 |
|---|---|---|---|---|---|---|
| 41250-058-30 | Diphenhydramine HCl and Zinc Acetate | 76 g in 1 CAN | SPRAY | 76 | 11 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| QIAN LI ZHUI FENG PAIN RELIEVING | CAMPHOR, MENTHOL, AND METHYL SALICYLATE | MADISON ONE ACME INC | 03a4fb7c-2328-409d-99c8-cbcf2b4a451f | 2025-11-10 | Warnings, Adverse reactions | M017 |
| WU YANG BRAND PAIN RELIEVING MEDICATED | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 05c6b95a-aeb6-4234-97c7-8d77eccb38d8 | 2025-11-10 | Warnings | M017 |
| HEI GUI PAIN RELIEVING | CAMPHOR AND METHYL SALICYLATE | MADISON ONE ACME INC | 4140c404-edab-4923-941d-f74125e943a9 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| E MEI SHAN MEDICATED | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | ddcc814e-fcc4-4232-9ab4-826b8aac35f0 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Overtime | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 25fec070-8587-42d1-ba6f-1a9c150acc98 | 2025-11-10 | Warnings | M017 |
| Dendracin Neurodendraxcin | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 05742cd5-ece2-4007-bdf0-46b76d23df74 | 2025-11-10 | Warnings | M017 |
| Anal Blu | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b9555b-c3ff-4baa-e063-6394a90afb2c | 2025-11-10 | Warnings | M017 |
| Stallion | DELAY CREME | Novelties by Nasswalk, Inc. | 0261ec88-8fe4-d5f8-e063-6294a90ab3d4 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b89eed-b433-a263-e063-6294a90a675b | 2025-11-10 | Warnings | M017 |
| Instant Erection | ULTIMATE ERECTION ENHANCER | Novelties by Nasswalk, Inc. | 03a444f9-7052-0c38-e063-6294a90a4e56 | 2025-11-10 | Warnings | M017 |
| STA-HARD | DESENSITIZING LUBRICANT | Novelties by Nasswalk, Inc. | 02ef794b-8e70-5c26-e063-6294a90a28d1 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03a4a7ce-4cff-a608-e063-6294a90ad65d | 2025-11-10 | Warnings | M017 |
| FOOTSPA PEDI | ALCOHOL | CHEMCO CORPORATION | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2025-11-08 | Warnings | M017 |
| Johnson and Johnson All Purpose First Aid Kit | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 5cdb47c5-7951-4279-8a05-0a3199d3dd45 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid Travel Ready 80 CT | ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f388f105-48ba-4616-e053-2a95a90a0049 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid All Purpose 160 CT | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f3933330-2550-4a88-e053-2a95a90a3997 | 2025-11-06 | Warnings | M017 |
| Foot and Leg Pain Relief | LIDOCAINE | Premier Brands of America Inc. | 42f23e2f-11c6-da49-e063-6294a90ac720 | 2025-11-06 | Warnings | M017 |
| HEALING TREE CALMING ANTI-ITCH | HYDROCORTISONE | Renu Laboratories, LLC | fc8bcde9-26e8-a35f-e053-6394a90a3300 | 2025-11-06 | Warnings | M017 |
| Calamine Plus | CALAMINE PLUS PRAMOXINE HCL | Chain Drug Marketing Association Inc | 1a3f8819-58cf-8923-e063-6394a90a37af | 2025-11-06 | Warnings | M017 |
| Extra Strength Itch Relief | DIPHENHYDRAMINE HCL AND ZINC ACETATE | Chain Drug Marketing Association Inc | 1a2997bc-7741-e658-e063-6394a90af6fd | 2025-11-06 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1053138 | diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray | PSN | 18998e1c-1254-4d0c-93f1-26652c5ca076 | 11 |
| 1053138 | diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray | SCD | 18998e1c-1254-4d0c-93f1-26652c5ca076 | 11 |
| 1053138 | diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray | SY | 18998e1c-1254-4d0c-93f1-26652c5ca076 | 11 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-058-30 | 41250005830 | 76 g in 1 CAN (41250-058-30) | 76 g | 2015-09-15 | 2027-05-31 | No | No | Current |