NDC 74307-010-01 - Underarm Antiperspirant PM Wipes Clean Lavender Scent
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
- 74307-010
- Requested NDC
- 74307-010-01
- Package NDCs from labels
- 74307-010-01, 74307-010-02
- Manufacturer
- Clutch Inc
- Effective date
- 2026-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Underarm Antiperspirant PM Wipes Clean Lavender Scent - Clutch Inc | Clutch Inc | 2026-08-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74307-010-01 | Underarm Antiperspirant PM Wipes Clean Lavender Scent | 106 g in 1 PACKAGE | SOLUTION | 106 | 3 | |
| 74307-010-02 | Underarm Antiperspirant PM Wipes Clean Lavender Scent | 15 in 1 JAR | SOLUTION | 15 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 74307-010 | UNDERARM ANTIPERSPIRANT PM WIPES CLEAN LAVENDER SCENT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) SOLUTION [CLUTCH INC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241115_d78ad43a-c225-0629-e053-2a95a90a3781.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.