Foaming Sanitizer
- Product NDC
- 71303-683
- Requested package NDC
- 71303-683-41
- 11-digit product format
- 713030683
- Labeler code
- 71303
- Product ID
- 71303-683_d6e7f5c4-0ffd-b02e-e053-2995a90ad219
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride 0.13%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RJ Schinner
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-03-30
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71303-683-41 | 71303068341 | 1000 mL in 1 BAG (71303-683-41) | 1000 ml | 2017-03-30 | 0000-00-00 | No | No | Current |