2 IN 1LAXATIVE STOOL SOFTENER AND STIULANT LAXATIVE
- Manufacturer
- RITE AID | TIME CAP LABORATORIES, INC.
- Effective date
- 2021-11-09
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:44:50
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients (in each tablet)
Docusate sodium 50 mg
Sennosides 8.6 mg
OTC - PURPOSE SECTION
Purposes
Stool softener
Stimulant laxative
INDICATIONS & USAGE SECTION
Uses
- relieves occasional constipation (irregularity)
- generally produces bowel movement in 6 to 12 hours
WARNINGS SECTION
Warnings
OTC - DO NOT USE SECTION
Do not use
- laxative products for longer than 1 week unless told to do so by a doctor
- if you are presently taking mineral oil, unless told to do so by a doctor
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have
- stomach pain
- nausea
- vomiting
- noticed a sudden change in bowel habits that lasts over 2 weeks
OTC - STOP USE SECTION
Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative.
These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
- take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses.
adults and children 12 years and older: take 2-4 tablets daily
children 6 to under 12 years of age: take 1-2 tablets daily
children 2 to under 6 years of age: take up to 1 tablet daily
children under 2 years: ask a doctor
OTHER SAFETY INFORMATION
Other information
- each tablet contains: calcium 20 mg, sodium 6 mg (VERY LOW SODIUM)
- store at 25°C (77°F) excursions permitted between 15°- 30°C (59°- 86°F)
INACTIVE INGREDIENT SECTION
Inactive ingredients carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, titanium dioxide
OTC - QUESTIONS SECTION
Questions or comments
call 1-877-290-4008
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 11822-3702-1 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a226-d83d-e063-dadaa90ab31f | 209R RITE AID 11822 3702 1 Laxative Stool Softener/Stimulant Laxative 400 Count |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11822-3702-1 | 2 IN 1LAXATIVE STOOL SOFTENER AND STIULANT LAXATIVE | 400 in 1 BOTTLE, PLASTIC | TABLET, COATED | 400 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11822-3702 | 2 IN 1LAXATIVE STOOL SOFTENER AND STIULANT LAXATIVE (STOOL SOFTENER-STIMULANT LAXATIVE) TABLET, COATED [RITE AID] | 2 | Legacy NDC, 1 package rows | 20211110_addc108a-ea97-9c87-e053-2995a90acbe4.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 11822-3702-1 | EA - Each | 11822-3702 | ac70343e-937c-4add-9e6a-7bb18f2cba5d | 1 | 2024-06-10 |
Products#
Every source-derived product name is available through these pages.
- 2 IN 1LAXATIVE STOOL SOFTENER AND STIULANT LAXATIVE
- STOOL SOFTENER-STIMULANT LAXATIVE
- SODIUM BENZOATE
- STEARIC ACID
- TITANIUM DIOXIDE
- CARNAUBA WAX
- CROSCARMELLOSE SODIUM
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- FD&C RED NO. 40
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- HYPROMELLOSE, UNSPECIFIED
- POLYETHYLENE GLYCOL, UNSPECIFIED
- DOCUSATE SODIUM
- DOCUSATE
- SENNOSIDES
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11822-3702 | 11822-3702-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| cfb70659-31e8-48f3-e053-2995a90ae6df | addc108a-ea97-9c87-e053-2995a90acbe4 | 2021-11-09 | Warnings | cfb70659-31e8-48f3-e053-2995a90ae6df addc108a-ea97-9c87-e053-2995a90acbe4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
