Antibacterial
- Product NDC
- 58575-507
- 11-digit product format
- 585750507
- Labeler code
- 58575
- Product ID
- 58575-507_7eee57d7-79a4-498d-937d-3743eae037c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chloroxylenol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Inopak, Ltd
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- CHLOROXYLENOL
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.