PFA STRONGHOLD HAND SANITIZER
- Product NDC
- 80969-001
- 11-digit product format
- 809690001
- Labeler code
- 80969
- Product ID
- 80969-001_c9797566-e51b-8f5f-e053-2a95a90ae74b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- STRONGHOLD TRADING LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-08-13
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80969-001-01 | PFA STRONGHOLD HAND SANITIZER | 60 mL in 1 BOTTLE | GEL | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80969-001 | PFA STRONGHOLD HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [STRONGHOLD TRADING LLC] | 1 | Legacy NDC, 1 package rows | 20210814_8af4767a-48d9-4c30-a0b9-baafcd19474e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80969-001-01 | 80969000101 | 60 mL in 1 BOTTLE (80969-001-01) | 60 ml | 2021-08-13 | 0000-00-00 | No | No | Current |