Instant Foaming Hand Sanitizer
- Product NDC
- 66608-207
- Requested package NDC
- 66608-207-78
- 11-digit product format
- 666080207
- Labeler code
- 66608
- Product ID
- 66608-207_d6e7f5c4-1003-b02e-e053-2995a90ad219
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Kimball Midwest
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-04-04
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|
| 2024-11-09 02:27 UTC · source 2024-11-08 | D | Discontinued by firm | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | D | Discontinued by firm | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | D | Discontinued by firm | 557ba5c1ecfa… | 9c80585c8c6e… |
| 2019-12-08 06:16 UTC · source 2019-12-05 | E | Excluded after deficient or non-compliant submission was not corrected | 110d247fa046… | a55b01930146… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 66608-207-78 | 66608020778 | 950 mL in 1 BOTTLE, PLASTIC (66608-207-78) | 950 ml | 2017-04-04 | 0000-00-00 | No | No | Current |