Antibacterial
- Product NDC
- 58575-512
- 11-digit product format
- 585750512
- Labeler code
- 58575
- Product ID
- 58575-512_9ecd4fcd-53eb-4bd1-a8c5-de6eb916e03b
- 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
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- CHLOROXYLENOL
- Active strength
- 3 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.