NDC 11429-1002-07 - FoamFresh E-2 Sanitizer Cleanser
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
- 11429-1002
- Requested NDC
- 11429-1002-07
- Package NDCs from labels
- 11429-1002-3, 11429-1002-7, 11429-1002-8, 11429-1002-6, 11429-1002-9, 11429-1002-0, 11429-1002-07
- Manufacturer
- Woodbine Products Company
- Effective date
- 2024-11-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FoamFresh E-2 Sanitizer Cleanser - Woodbine Products Company | Woodbine Products Company | 2024-11-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11429-1002-0 | FoamFresh E-2 Sanitizer Cleanser | 1125 mL in 1 BOTTLE | LIQUID | 1125 | 5 | |
| 11429-1002-3 | FoamFresh E-2 Sanitizer Cleanser | 1000 mL in 1 BOTTLE, PLASTIC | LIQUID | 1000 | 5 | |
| 11429-1002-6 | FoamFresh E-2 Sanitizer Cleanser | 3785 mL in 1 BOTTLE | LIQUID | 3785 | 5 | |
| 11429-1002-7 | FoamFresh E-2 Sanitizer Cleanser | 750 mL in 1 BOTTLE, PLASTIC | LIQUID | 750 | 5 | |
| 11429-1002-8 | FoamFresh E-2 Sanitizer Cleanser | 1250 mL in 1 BOTTLE, PLASTIC | LIQUID | 1250 | 5 | |
| 11429-1002-9 | FoamFresh E-2 Sanitizer Cleanser | 1100 mL in 1 BOTTLE | LIQUID | 1100 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11429-1002 | FOAMFRESH E-2 SANITIZER CLEANSER (BENZALKONIUM CHLORIDE) LIQUID [WOODBINE PRODUCTS COMPANY] | 5 | Current NDC, Legacy NDC, 6 package rows | 20241127_c49f49ad-06fc-4759-9ac9-1f1e29d8c2cf.zip |
DailyMed Socrata Ingredients#
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.