Hand Sanitizer
- Product NDC
- 76835-002
- Requested package NDC
- 76835-002-03
- 11-digit product format
- 768350002
- Labeler code
- 76835
- Product ID
- 76835-002_f1f01b41-eeb5-09b1-e053-2a95a90a1c40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Isopropyl Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Siebert Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ISOPROPYL ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|---|---|---|---|---|---|---|---|
| 76835-002-03 | 76835000203 | 236 mL in 1 BOTTLE, PLASTIC (76835-002-03) | 236 ml | 2020-06-04 | 0000-00-00 | No | No | Current |