Hand Sanitizer Pure Experience Liquid
- Product NDC
- 70956-312
- 11-digit product format
- 709560312
- Labeler code
- 70956
- Product ID
- 70956-312_9e8ac697-4a14-4b62-ba4b-8fcb1bdbe1a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Absara Cosmetics S.A.P.I DE C.V.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- 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 |
|---|
| 70956-312-01 | 70956031201 | 60 mL in 1 BOTTLE (70956-312-01) | 60 ml | 2020-06-01 | 0000-00-00 | No | No | Current |
| 70956-312-04 | 70956031204 | 500 mL in 1 BOTTLE (70956-312-04) | 500 ml | 2020-06-01 | 0000-00-00 | No | No | Current |
| 70956-312-08 | 70956031208 | 3780 mL in 1 BOTTLE (70956-312-08) | 3780 ml | 2020-06-01 | 0000-00-00 | No | No | Current |