CoreTex Antibacterial Hand Sanitizer
- Product NDC
- 65753-200
- Requested package NDC
- 65753-200-32
- 11-digit product format
- 657530200
- Labeler code
- 65753
- Product ID
- 65753-200_f166c49c-4650-afa5-e053-2995a90a4ba2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SD alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- CoreTex Products Inc
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-11-25
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 63 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 65753-200 | 65753-200-32 | D | Discontinued by firm | 2026-10-05 |
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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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 |
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 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 RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1043353 | benzocaine 6 % Medicated Pad | PSN | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263170 | camphor 0.1 % / diphenhydrAMINE HCl 2 % / zinc acetate 1 % Topical Gel | PSN | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1039474 | ethanol 62.5 % Topical Solution | PSN | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263166 | StingX 6 % Topical Swab | PSN | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263166 | benzocaine 60 MG/ML Medicated Pad [StingX] | SBD | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1043353 | benzocaine 60 MG/ML Medicated Pad | SCD | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263170 | camphor 0.001 MG/MG / diphenhydramine hydrochloride 0.02 MG/MG / zinc acetate 0.01 MG/MG Topical Gel | SCD | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1039474 | ethanol 0.625 ML/ML Topical Solution | SCD | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1043353 | benzocaine 6 % Medicated Wipe | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1043353 | benzocaine 6 % Topical Swab | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263170 | camphor 0.001 MG/MG / diphenhydramine HCl 0.02 MG/MG / zinc acetate 0.01 MG/MG Topical Gel | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263170 | camphor 0.1 % / diphenhydramine HCl 2 % / zinc acetate 1 % Topical Gel | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 1039474 | ethanol 62.5 % Topical Solution | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
| 2263166 | StingX 60 MG/ML Medicated Pad | SY | 095855ef-85f5-dacd-e063-6294a90a597c | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 65753-200-32 | 65753020032 | 44 mL in 1 BOTTLE (65753-200-32) | 44 ml | 2019-11-26 | 0000-00-00 | No | No | Current |