PFA FOR HAND SANITIZER
- Product NDC
- 80969-030
- 11-digit product format
- 809690030
- Labeler code
- 80969
- Product ID
- 80969-030_c9f47d5c-0f1a-2348-e053-2a95a90a1dbd
- 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
- 2021-08-03
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80969-030-02 | 80969003002 | 60 mL in 1 BOTTLE (80969-030-02) | 60 ml | 2021-08-03 | 0000-00-00 | No | No | Current |