NDC 76887-102-01 - Puretize Instant Hand Sanitizer 500ml
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 76887-102
- Requested NDC
- 76887-102-01
- Package NDCs from labels
- 76887-102-01, 76887-102-02
- Manufacturer
- ARGO KOREA Co., Ltd | E.CIS COSMETIC.Co.,Ltd
- Effective date
- 2020-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ethyl Alcohol - ARGO KOREA Co., Ltd | E.CIS COSMETIC.Co.,Ltd | ARGO KOREA Co., Ltd | E.CIS COSMETIC.Co.,Ltd | 2020-05-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 76887-102-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-dac5-a426-e053-dadaa90af4c2 | PURETIZE INSTANT HAND SANITIZER 70% 500ml |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76887-102-01 | Puretize Instant Hand Sanitizer 500ml | 500 mL in 1 BOTTLE, PUMP | GEL | 500 | 3 | |
| 76887-102-02 | Puretize Instant Hand Sanitizer 500ml | 24 in 1 CARTON | GEL | 24 | 3 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.