KOBOInstant Hand Sanitizer
- Product NDC
- 42001-001
- 11-digit product format
- 420010001
- Labeler code
- 42001
- Product ID
- 42001-001_a3cb2182-54d4-3643-e053-2a95a90a3806
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- KOBOInstant Hand Sanitizer
- Dosage form
- LIQUID
- Route
- EXTRACORPOREAL
- Labeler
- KOBO Cosmetics Co., Ltd.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-21
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 375 mL/500mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42001-001-01 | 42001000101 | 500 mL in 1 BOTTLE (42001-001-01) | 500 ml | 2020-04-21 | 0000-00-00 | No | No | Current |