Docusate Sodium Oral Liquid
- Product NDC
- 81033-022
- 11-digit product format
- 810330022
- Labeler code
- 81033
- Product ID
- 81033-022_331277b8-8305-d082-e063-6394a90a4dd3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium Oral Liquid
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Kesin Pharma Corporation
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-04-01
- Substance
- DOCUSATE SODIUM
- Active strength
- 100 mg/10mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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
- Docusate Sodium Oral Liquid
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DOCUSATE SODIUM | 100 mg/10mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| F05Q2T2JA0 | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1248119 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 331277b8-8304-d082-e063-6394a90a4dd3 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| 6084a4f4-5437-c9a5-caec-5361ee075a59 | Product name | 1 | 20140508 |
| 90c5639a-61b0-88d6-ddcf-21888e94869a | Product name | 1 | 20140508 |
| 9514609b-a2a9-f8ec-6ba6-3f8e5ee89877 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-022-10 | Docusate Sodium Oral Liquid | 10 mL in 1 CUP, UNIT-DOSE | LIQUID | 10 | 1 | |
| 81033-022-50 | Docusate Sodium Oral Liquid | 100 in 1 CASE | LIQUID | 100 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-022-10 | ML - Milliliter | 81033-022 | 592e48d2-2f24-4f2f-b824-d15fadcaf4be | 1 | 2025-05-14 |
| 81033-022-50 | ML - Milliliter | 81033-022 | 2088ee40-f975-4ca9-b2a3-65a3d1971428 | 1 | 2025-05-14 |
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 |
|---|---|---|---|---|---|---|
| up and up fiber therapy | PSYLLIUM HUSK | Target Corporation | 674753ee-1174-4c06-9ed3-a090b338a39e | 2025-11-05 | Warnings | M007 |
| up and up fiber therapy | PSYLLIUM HUSK | TARGET CORPORATION | 956c48f8-c705-4a86-9866-c68a48ddeb6c | 2025-11-05 | Warnings | M007 |
| CEO-TWO | LAXATIVE | Beutlich Pharmaceuticals, LLC | 08670636-5795-4db0-e063-6294a90afa4b | 2025-11-05 | Warnings | M007 |
| up and up gentle laxative | BISACODYL | Target Corporation | 4a29dc2b-b68f-471b-a84e-4a5096aa3748 | 2025-11-04 | Warnings | M007 |
| Target Fiber Laxative | PSYLLIUM HUSK | TARGET CORPORATION | a581116a-392d-4ac3-ae15-4318506a7b2a | 2025-11-04 | Warnings | M007 |
| up and up fiber therapy | CALCIUM POLYCARBOPHIL | Target Corporation. | e5473950-06f4-4ea4-975b-3ac94957e776 | 2025-11-04 | Warnings | M007 |
| up and up fiber therapy Natural Fiber | PSYLLIUM HUSK | Target Corporation | f8b1c831-6fd0-4a58-9726-4e0f986c8084 | 2025-11-04 | Warnings | M007 |
| OneLAX | BISACODYL | AKRON PHARMA INC | be4eeb4d-df29-45dc-94ff-933e52c8b6f6 | 2025-11-03 | Warnings | M007 |
| Gentle Stool Softener | DOCUSATE SODIUM | WALGREEN COMPANY | 169b33f9-e559-47bf-bbba-c7eda4762c7f | 2025-10-31 | Warnings | M007 |
| Senna S | DOCUSATE SODIUM, SENNOSIDES | Walgreens | 765bfd9b-7a21-4315-9add-cf13007722d5 | 2025-10-31 | Warnings | M007 |
| Gentle Stool Softener | DOCUSATE SODIUM | WALGREEN COMPANY | 71b15339-2585-4fae-8445-6fbb4f0a378e | 2025-10-31 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Major Pharmaceuticals | 97561cd4-63d9-44c2-a3a3-ec668a09a4ed | 2025-10-31 | Warnings | M007 |
| Fiber Caplets | CALCIUM POLYCARBOPHIL | SAFEWAY | 08e2e8b0-90b3-48d6-a72a-40688c74771a | 2025-10-29 | Warnings | M007 |
| Glycerin | GLYCERIN | Chain Drug Marketing Association Inc. | 424d91f0-ecf9-6d9b-e063-6394a90a8006 | 2025-10-29 | Warnings | M007 |
| Publix Laxative Maximum Strength | CALCIUM SENNOSIDES | PUBLIX SUPER MARKETS, INC | 11112859-ef1e-4b37-9915-ba4d06a3f198 | 2025-10-28 | Warnings | M007 |
| Publix Stimulant Laxative | BISACODYL | PUBLIX SUPER MARKETS, INC | 02e596a7-b8e5-4f55-9bc6-6d17e0fabda7 | 2025-10-28 | Warnings | M007 |
| PUBLIX | PSYLLIUM HUSK | PUBLIX SUPER MARKETS, INC | 55f98d3f-f282-4f19-b373-0b59640d274d | 2025-10-28 | Warnings | M007 |
| PUBLIX | CALCIUM POLYCARBOPHIL | PUBLIX SUPER MARKETS, INC | 02e3f4ce-8961-425c-98a9-3b9d66709ca5 | 2025-10-28 | Warnings | M007 |
| Publix Women Laxative | BISACODYL | PUBLIX SUPER MARKETS, INC | 03eeca55-f239-4a01-a900-c1943f27a834 | 2025-10-28 | Warnings | M007 |
| Publix Fiber Therapy Orange Smooth | PSYLLIUM HUSK | PUBLIX SUPER MARKETS, INC | b9c54c20-cd82-4627-9217-a66834db4799 | 2025-10-28 | Warnings | M007 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1248119 | docusate sodium 50 MG in 5 mL Oral Suspension | PSN | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
| 1248119 | docusate sodium 10 MG/ML Oral Suspension | SCD | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
| 1248119 | docusate sodium 100 MG per 10 ML Oral Suspension | SY | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
| 1248119 | docusate sodium 150 MG per 15 ML Oral Suspension | SY | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
| 1248119 | docusate sodium 50 MG per 5 ML Oral Suspension | SY | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
| 1248119 | DOSS Sodium 10 MG/ML Oral Suspension | SY | 331277b8-8304-d082-e063-6394a90a4dd3 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 81033-022-10 | 81033002210 | 10 mL in 1 CUP, UNIT-DOSE | 10 ml | Historical | |||
| 81033-022-50 | 81033002250 | 100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10) | 2025-04-01 | No | No | Current |