Hand Sanitizer
- Product NDC
- 80710-213
- 11-digit product format
- 807100213
- Labeler code
- 80710
- Product ID
- 80710-213_ea4d87bf-70c3-5abf-e053-2a95a90aad11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- D3W Industries Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 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 product | product | 80710-213 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 80710-213 | 80710-213-05 | D | Discontinued by firm | 2026-10-15 | |
| excluded package | package | 80710-213 | 80710-213-64 | D | Discontinued by firm | 2026-10-15 |
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 | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 80710-213-64 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 80710-213-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 80710-213-64 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 80710-213-05 | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 80710-213-02 | 80710021302 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-02) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-04 | 80710021304 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-04) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-08 | 80710021308 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-08) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-16 | 80710021316 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-16) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-32 | 80710021332 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-32) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-60 | 80710021360 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-60) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-64 | 80710021364 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-64) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |
| 80710-213-70 | 80710021370 | 0 mL in 1 BOTTLE, PLASTIC (80710-213-70) | 0 ml | 2020-10-06 | 0000-00-00 | No | No | Current |