Ecolab
- Product NDC
- 63146-122
- Requested package NDC
- 63146-122-11
- 11-digit product format
- 631460122
- Labeler code
- 63146
- Product ID
- 63146-122_ea772fad-366e-4820-975e-bcac5c166509
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Kay Chemical Company
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-02-18
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 20 mg/mL
- 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 package | package | 63146-122 | 63146-122-11 | D | Discontinued by firm | 2026-11-06 |
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 |
|---|---|---|---|---|---|---|---|---|
| 63146-122-11 | 63146012211 | 2000 mL in 1 BOTTLE, PLASTIC (63146-122-11) | 2000 ml | 2016-02-18 | 0000-00-00 | No | No | Current |