Womens Laxative
- Product NDC
- 37808-676
- 11-digit product format
- 378080676
- Labeler code
- 37808
- Product ID
- 37808-676_2a3c57e4-8fb1-4e1a-87bf-293567e923ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bisacodyl
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-09-16
- Marketing end
- 0000-00-00
- Substance
- BISACODYL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37808-676-11 | Womens Laxative | 15 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 15 | | 15 |
| 37808-676-11 | Womens Laxative | 4 in 1 CARTON | TABLET, DELAYED RELEASE | 4 | | 15 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-676 | WOMENS LAXATIVE (BISACODYL) TABLET, DELAYED RELEASE [H E B] | 14 | Legacy NDC, 2 package rows | 20240825_7a741a60-558b-4bdc-9e07-0bc572962163.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-676-11 | 37808067611 | 4 BLISTER PACK in 1 CARTON (37808-676-11) > 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 4 blister pack | 2015-09-16 | 0000-00-00 | No | No | Current |