JEKSUNG
- Product NDC
- 55451-006
- 11-digit product format
- 554510006
- Labeler code
- 55451
- Product ID
- 55451-006_a3db77f8-0cd8-0909-e053-2a95a90a90a6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SKIN REPAIR
- Dosage form
- LIQUID
- Route
- EXTRACORPOREAL
- Labeler
- Zhejiang Shiao Technology Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-01-21
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE; QUATERNIUM-16; CLOTRIMAZOLE
- Active strength
- 0 mg/30mL; mg/30mL; mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record