Antibacterial
- Product NDC
- 52380-1865
- 11-digit product format
- 523801865
- Labeler code
- 52380
- Product ID
- 52380-1865_9d4d66f7-fa47-e832-e053-2a95a90a8b62
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triclosan
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Aplicare Products, LLC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1998-09-01
- Marketing end
- 2020-07-01
- Substance
- TRICLOSAN
- Active strength
- 0 g/100g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record