NDC 85138-101-01 - MENOW SUNSCREEN
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
- 85138-101
- Requested NDC
- 85138-101-01
- Package NDCs from labels
- 85138-101-01, 85138-101-02
- Manufacturer
- SHANTOU QIWEI INDUSTRY CO.,LTD
- Effective date
- 2025-01-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MENOW SUNSCREEN - SHANTOU QIWEI INDUSTRY CO.,LTD | SHANTOU QIWEI INDUSTRY CO.,LTD | 2025-01-17 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85138-101-01 | MENOW SUNSCREEN | 9 g in 1 BOX | POWDER | 9 | 1 | |
| 85138-101-02 | MENOW SUNSCREEN | 1 in 1 BOX | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 85138-101 | MENOW SUNSCREEN (ETHYLHEXYL METHOXYCINNAMATE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, ZINC OXIDE, TITANIUM DIOXIDE) POWDER [SHANTOU QIWEI INDUSTRY CO.,LTD] | 1 | 2 package rows | 20250121_2be1dfce-1881-aab3-e063-6394a90ac464.zip |
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.