Laxative
- Product NDC
- 37808-779
- Requested package NDC
- 37808-779-08
- 11-digit product format
- 378080779
- Labeler code
- 37808
- Product ID
- 37808-779_96ebf703-a8e8-485f-a5ec-0789c5a05106
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sennosides
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- H E B
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-13
- Substance
- SENNOSIDES
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Laxative
- Brand name suffix
- Maximum Strength
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SENNOSIDES | 25 mg/1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 37808-779-08 | 37808077908 | 2 BLISTER PACK in 1 CARTON (37808-779-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2026-10-13 | No | No | Current |