Pure and Protected Sand Sanitizing Foam
- Product NDC
- 77506-002
- 11-digit product format
- 775060002
- Labeler code
- 77506
- Product ID
- 77506-002_afe8da18-96ca-9612-e053-2a95a90a8d39
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Uniters SPA
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-06
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/100mL
- 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 |
|---|
| 77506-002-08 | 77506000208 | 50 mL in 1 BOTTLE, PUMP (77506-002-08) | 50 ml | 2020-08-06 | 0000-00-00 | No | No | Current |
| 77506-002-12 | 77506000212 | 100 mL in 1 BOTTLE, PUMP (77506-002-12) | 100 ml | 2020-08-06 | 0000-00-00 | No | No | Current |
| 77506-002-15 | 77506000215 | 200 mL in 1 BOTTLE, PUMP (77506-002-15) | 200 ml | 2020-08-06 | 0000-00-00 | No | No | Current |
| 77506-002-36 | 77506000236 | 1000000 mL in 1 TANK (77506-002-36) | 1000000 ml | 2020-09-22 | 0000-00-00 | No | No | Current |