NDC 74441-101-01 - PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml
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
- 74441-101
- Requested NDC
- 74441-101-01
- Package NDCs from labels
- 74441-101-01, 74441-101-02
- Manufacturer
- Visage Cosmetic Co., Ltd | E.CIS Cosmetic Co.,Ltd
- Effective date
- 2020-05-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ethyl Alcohol - Visage Cosmetic Co., Ltd | E.CIS Cosmetic Co.,Ltd | Visage Cosmetic Co., Ltd | E.CIS Cosmetic Co.,Ltd | 2020-05-25 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74441-101-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-f560-a426-e053-dadaa90af4c2 | PLUS BEAU VISAGE Hand Sanitizing Gel 62% 250ml |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74441-101-01 | PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml | 250 mL in 1 BOTTLE | LIQUID | 250 | 3 | |
| 74441-101-02 | PLUSBEAU VISAGE Hand Sanitizing Gel 62% 250ml | 30 in 1 CASE | LIQUID | 30 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CVS Hand Sanitizer | ALCOHOL | CVS | d0081c50-c0d2-436a-ba83-5d1982ae64b7 | 2015-08-17 | Warnings | 3K9958V90M |
| Instant Hand Sanitizer | ALCOHOL | Safetec of America, Inc. | f9e30645-491b-4f54-acfd-f863ee235607 | 2013-08-07 | Warnings | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.