Protex Hand Sanitizer
- Product NDC
- 30775-040
- 11-digit product format
- 307750040
- Labeler code
- 30775
- Product ID
- 30775-040_ef52e9fb-21d0-f674-e053-2995a90a644a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Foaming Hand Sanitizer
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Parker Laboratories, Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-03-31
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 30775-040-02 | 30775004002 | 24 BOTTLE in 1 BOX (30775-040-02) > 60 g in 1 BOTTLE | 24 bottle | 2021-03-31 | 0000-00-00 | No | No | Current |
| 30775-040-18 | 30775004018 | 2 BOX in 1 BOX (30775-040-18) > 8 BOTTLE in 1 BOX > 550 g in 1 BOTTLE | 2 box | 2021-03-31 | 0000-00-00 | No | No | Current |