NDC 70936-202 - HEXASORB UNDERPADS
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
- 70936-202
- Package NDCs from labels
- 70936-202-01, 70936-202-11, 70936-202-10
- Manufacturer
- SMART CHOICE MEDICAL INC.
- Effective date
- 2018-01-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HEXASORB UNDERPADS | SMART CHOICE MEDICAL INC. | 2018-01-19 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70936-202-01 | HEXASORB UNDERPADS | 1 in 1 PACKAGE | 1 | 5 | ||
| 70936-202-10 | HEXASORB UNDERPADS | 10 in 1 PACKAGE | 10 | 5 | ||
| 70936-202-11 | HEXASORB UNDERPADS | 100 in 1 CASE | 100 | 5 |
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 |
|---|---|---|---|---|---|---|
| AVANCE ALOE INCONTINENCE CARE | DIMETICONE | SMART CHOICE MEDICAL INC. | 558d239e-b0cf-c145-e063-6294a90a8a8b | 2026-07-01 | Warnings | SMART CHOICE MEDICAL INC. |
| AVANCE ALOE INCONTINENCE CARE | DIMETICONE | SMART CHOICE MEDICAL INC. | 55833e0f-d184-16a2-e063-6394a90acfd3 | 2026-06-30 | Warnings | SMART CHOICE MEDICAL INC. |
| AVANCE INCONTINENCE CARE | BENZETHONIUM CHLORIDE | SMART CHOICE MEDICAL INC. | e2c51699-d4da-5b88-e053-2995a90afd7f | 2026-01-12 | Warnings | SMART CHOICE MEDICAL INC. |
| AVANCE INCONTINENCE CARE | BENZETHONIUM CHLORIDE | SMART CHOICE MEDICAL INC. | e297b705-8070-f7c3-e053-2a95a90a8c5b | 2026-01-12 | Warnings | SMART CHOICE MEDICAL INC. |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.