Hand Sanitizer
- Product NDC
- 50814-051
- Requested package NDC
- 50814-051-02
- 11-digit product format
- 508140051
- Labeler code
- 50814
- Product ID
- 50814-051_a5f0cc00-a838-0aeb-e053-2995a90ae63b
- 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
- 2020-03-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 | 50814-051 | 50814-051-02 | 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50814-051-02 | 50814005102 | 200 mL in 1 BOTTLE (50814-051-02) | 200 ml | 2020-03-01 | 0000-00-00 | No | No | Current |