Apres Foaming Hand Sanitizer
- Product NDC
- 42326-580
- 11-digit product format
- 423260580
- Labeler code
- 42326
- Product ID
- 42326-580_b5f711ee-90d9-091c-e053-2a95a90a77cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Petra Hygienic Systems International Limited
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-12-07
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42326-580 | APRES FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [PETRA HYGIENIC SYSTEMS INTERNATIONAL LIMITED] | 3 | Legacy NDC | 20250210_b5f707c4-699d-0c9e-e053-2995a90aa934.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42326-580-01 | 42326058001 | 3700 mL in 1 BOTTLE (42326-580-01) | 3700 ml | 2020-12-07 | 0000-00-00 | No | No | Current |