NEORELIEF HAND SANITIZER
- Product NDC
- 58368-007
- Requested package NDC
- 58368-007-01
- 11-digit product format
- 583680007
- Labeler code
- 58368
- Product ID
- 58368-007_edab70c3-d209-6afb-e053-2a95a90ab51e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- NEORELIEF HAND SANITIZER
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- BioLyte Laboratories, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-29
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|---|---|---|---|---|---|---|---|
| 58368-007-01 | 58368000701 | 60 mL in 1 BOTTLE, PLASTIC (58368-007-01) | 60 ml | 2020-06-29 | 0000-00-00 | No | No | Current |