Refill 2
- Product NDC
- 50814-016
- 11-digit product format
- 508140016
- Labeler code
- 50814
- Product ID
- 50814-016_83716894-42d6-8de2-e053-2a91aa0a0fe6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
- Dosage form
- KIT
- Labeler
- GFA Production (Xiamen) Co., Ltd.
- Application
- part333B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-08-10
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | 50814-016 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 50814-016 | 50814-016-01 | 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50814-016-01 | 50814001601 | 1 KIT in 1 KIT (50814-016-01) * 1 BOX in 1 BOX (50814-013-01) > 10 PACKET in 1 BOX > .9 g in 1 PACKET * 2 BOX in 1 BOX (50814-011-01) > 10 PATCH in 1 BOX > .9 g in 1 PATCH | 1 kit | 2016-08-10 | 0000-00-00 | No | No | Current |