Antiseptic Hand Sanitizer
- Product NDC
- 50814-008
- 11-digit product format
- 508140008
- Labeler code
- 50814
- Product ID
- 50814-008_b8f3494a-aa87-5827-e053-2a95a90ae53d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- GFA Production (Xiamen) Co., Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-07-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | 50814-008 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 50814-008 | 50814-008-01 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 50814-008-01 | 50814000801 | .81 mL in 1 BAG (50814-008-01) | 2016-07-01 | 0000-00-00 | No | No | Current |