FEVIA Constipation Control
- Product NDC
- 82706-029
- 11-digit product format
- 827060029
- Labeler code
- 82706
- Product ID
- 82706-029_4bd2fcec-955b-00a0-e063-6294a90a22c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- VIVUNT PHARMA LLC
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-19
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FEVIA Constipation Control
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0 |
| Rxcui | 1115005 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82706-029-01 | FEVIA Constipation Control | 50 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 50 | | 2 |
| 82706-029-01 | FEVIA Constipation Control | 1 in 1 CARTON | CAPSULE, LIQUID FILLED | 1 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82706-029-01 | 82706002901 | 1 BOTTLE in 1 CARTON (82706-029-01) / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2026-02-19 | No | No | Current |