Industrial Itch and Pain Relief
- Product NDC
- 59555-002
- 11-digit product format
- 595550002
- Labeler code
- 59555
- Product ID
- 59555-002_834e7e81-dbe6-40e9-a053-47a4b4423602
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- R & R Lotion, Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-05-01
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
- Active strength
- 20; 1 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
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 59555-002-19 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 59555-002-18 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 59555-002-19 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 59555-002-18 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 59555-002-19 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 59555-002-18 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 59555-002-19 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 59555-002-18 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 59555-002-19 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 59555-002-18 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 59555-002-18 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 59555-002-19 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 59555-002-18 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 59555-002-19 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 59555-002-18 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 59555-002-19 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
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
- Industrial Itch and Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 20 mg/mL |
| ZINC ACETATE | 1 mg/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| TC2D6JAD40 | Internal UNII lookup |
| FM5526K07A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1294589 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 236415fc-f923-4a82-b54a-ecaf666dd2e0 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 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 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 59555-002-18 | 2025-09-11 | Industrial Itch and Pain Relief |
| 59555-002-19 | 2025-09-11 | Industrial Itch and Pain Relief |
| 59555-002-18 | 2025-01-30 | Industrial Itch and Pain Relief |
| 59555-002-19 | 2025-01-30 | Industrial Itch and Pain Relief |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59555-002-18 | Industrial Itch and Pain Relief | 1 mL in 1 PACKET | LIQUID | 1 | 3 | |
| 59555-002-19 | Industrial Itch and Pain Relief | 20 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 20 | 3 |
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 |
|---|---|---|---|---|---|---|
| Numbsure LIDOCAINE | LIDOCAINE 4% | Hambli Limited | 43a65a12-ef2a-4608-e063-6394a90a82ea | 2026-01-31 | Warnings | M017 |
| Collajoint Lidocaine Pain Relief Gel Patch | LIDOCAINE PAIN RELIEF GEL PATCH | Henan Enokon Medical Instrument Co., Ltd. | 44e27e7f-992f-d194-e063-6294a90a94e4 | 2026-01-31 | Warnings | M017 |
| CAPSAICIN HEAT Patch | CAPSAICIN HEAT PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49ac2045-2c07-af9a-e063-6294a90a052a | 2026-01-31 | Warnings | M017 |
| COLD AND HOT MEDICATED Patch | COLD AND HOT MEDICATED PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49ac6a7b-25d3-6dc4-e063-6394a90a99b6 | 2026-01-31 | Warnings | M017 |
| COLD AND HOT MEDICATED Patch | COLD AND HOT MEDICATED PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49aca763-be2a-cf38-e063-6294a90a092e | 2026-01-31 | Warnings | M017 |
| PAIN RELIEF HOT Patch | PAIN RELIEF HOT PATCH | Henan Enokon Medical Instrument Co., Ltd. | 49ad128a-0f4c-085a-e063-6294a90ac9bb | 2026-01-31 | Warnings | M017 |
| Walgreens Chest Rub | CAMPHOR, EUCALYPTUS OIL, MENTHOL | Walgreen Company | 3557d2e9-714a-4066-aa73-ea9e3363e574 | 2026-01-30 | Warnings | M017 |
| Alveora HEMORRHOID MASTER | LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID MASTER | Jiangxi Yudexi Pharmaceutical Co., LTD | 4996f96a-898e-de01-e063-6394a90a3907 | 2026-01-30 | Warnings | M017 |
| Sunburn Relief | LIDOCAINE HCL 0.5% | Rite Aid Corporation | b67af0c7-1ae8-4494-bb0e-d7f66ebca352 | 2026-01-30 | Warnings, Adverse reactions | M017 |
| Drs Pharmacy PAIN RELIEF MUSCLE ARITHRITIS | CAPSAICIN | OL PHARMA TECH,LLC | 48fdf9dc-05df-866d-e063-6294a90ae03a | 2026-01-30 | Warnings | M017 |
| ROCKTAPE GO Kinesiology Tape and Analgesic | MENTHOL, METHYL SALICYLATE | Implus Footcare, LLC | b779c7d8-dbe6-472f-9282-6cced25cfd2e | 2026-01-29 | Warnings | M017 |
| RockSauce Warming Massage | MENTHOL, METHYL SALICYLATE | Implus Footcare, LLC | de5f7add-1f2b-438a-ac17-753ebb53e697 | 2026-01-29 | Warnings | M017 |
| RockSauce Warming Massage Roll-On | MENTHOL, METHYL SALICYLATE | Implus Footcare, LLC | 5a2d9c3a-67fc-4c1a-b1e8-62a93880397a | 2026-01-29 | Warnings | M017 |
| Analgesic Dr. Collado | MENTHOL, METHYL SALICYLATE | Laboratorios Dr. Collado, S.A | c0dad2db-7c96-49b8-a451-bf8cfa7f798b | 2026-01-29 | Warnings | M017 |
| RockSauce Warming Massage | MENTHOL, METHYL SALICYLATE | Implus Footcare, LLC | 3121c7f7-d7e5-4ca9-9057-03edf9c94c56 | 2026-01-29 | Warnings | M017 |
| Analgesic Gel Dr. Collado Menthol 4 Methyl Salicylate | MENTHOL, METHYL SALICYLATE | Laboratorios Dr. Collado, S.A. | 87c22e6f-3ab0-47c3-94ea-48b3d1a95d9d | 2026-01-29 | Warnings | M017 |
| ProCure Hydrocortisone Cream Plus | HYDROCORTISONE | Rooftop Consumer Health, Inc. | fe334cae-e019-4397-8498-df3c923ae8b5 | 2026-01-29 | Warnings | M017 |
| Red Oil Pain Relief | CAMPHOR (SYNTHETIC), MENTHOL, PHENOL | The Red Oil Company Inc | 1e36579a-72da-46ba-ac72-5960a11c0880 | 2026-01-29 | Warnings | M017 |
| Extra Strength Balm | CAPSICUM, MENTHOL | NATURES FORMULAE HEALTH PRODUCTS LTD. | 498a5e2a-4de0-561c-e063-6394a90ac05c | 2026-01-29 | Warnings | M017 |
| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET POTENT PAIN RELIEF | 45c76956-db3f-3e84-e063-6394a90adce1 | 2026-01-29 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1294589 | diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Solution | PSN | 236415fc-f923-4a82-b54a-ecaf666dd2e0 | 3 |
| 1294589 | diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution | SCD | 236415fc-f923-4a82-b54a-ecaf666dd2e0 | 3 |
| 1294589 | diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Solution | SY | 236415fc-f923-4a82-b54a-ecaf666dd2e0 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 59555-002-18 | 59555000218 | 1 mL in 1 PACKET (59555-002-18) | 1 ml | 2019-05-01 | 0000-00-00 | No | No | Current |
| 59555-002-19 | 59555000219 | 20 mL in 1 BOTTLE, WITH APPLICATOR (59555-002-19) | 20 ml | 2019-05-01 | 0000-00-00 | No | No | Current |