CLOROX Hand sanitizer Gel
- Product NDC
- 80714-034
- Requested package NDC
- 80714-034-10
- 11-digit product format
- 807140034
- Labeler code
- 80714
- Product ID
- 80714-034_dd980b15-f4f2-6325-e053-2a95a90ac5d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol hand Sanitizer
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- New Wave Global Services Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- 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 |
|---|---|---|---|---|---|---|---|---|
| 80714-034-10 | 80714003410 | 354 mL in 1 BOTTLE, PUMP (80714-034-10) | 354 ml | 2021-05-25 | 0000-00-00 | No | No | Current |