Vytis Shield Aloe Vera Foam Hand Sanitizer
- Product NDC
- 70299-001
- 11-digit product format
- 702990001
- Labeler code
- 70299
- Product ID
- 70299-001_7f1faf08-d6bb-593e-e053-2991aa0a94af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Vytis Shield, Llc
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-12-03
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 70299-001-00 | 70299000100 | 1 BOTTLE in 1 BOX (70299-001-00) > 50 mL in 1 BOTTLE | 1 bottle | 2015-12-03 | 0000-00-00 | No | No | Current |
| 70299-001-01 | 70299000101 | 1 BOTTLE in 1 BOX (70299-001-01) > 236 mL in 1 BOTTLE | 1 bottle | 2015-12-03 | 0000-00-00 | No | No | Current |
| 70299-001-02 | 70299000102 | 1 BOTTLE in 1 BOX (70299-001-02) > 1000 mL in 1 BOTTLE | 1 bottle | 2015-12-03 | 0000-00-00 | No | No | Current |