Over-the-counter drug · OTC MONOGRAPH DRUG
Stimulant Laxative Plus Stool Softener NDC 17856-1248
docusate sodium 50 mg and sennosides 8.6 mg · Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 · Tablet, Film coated · Oral · ATLANTIC BIOLOGICALS CORP.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 17856-1248-1 | 1785612480117856124801 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-1248-1) / 1 TABLET, FILM COATED in 1 POUCHMarketed from May 9, 2024 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Stimulant Laxative Plus Stool Softener
- Generic name (nonproprietary)
- docusate sodium 50 mg and sennosides 8.6 mg
- Active ingredients
- Sennosides — 8.6 mg/1Docusate sodium — 50 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- ATLANTIC BIOLOGICALS CORP.NDC labeler code 17856
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M
- Marketing start
- Listing expires
- Identifiers
- Product ID 17856-1248_38930b8a-9e76-2025-e063-6394a90a2478SPL ID 38930b8a-9e76-2025-e063-6394a90a2478SPL set ID 4c02fcec-6bb7-4497-96c5-0d809209dd17RxCUI 998740UNII 3FYP5M0IJX, F05Q2T2JA0
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N417856124801followed by a unit qualifier and the quantityPackage 17856-1248-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses relieves occasional constipation (irregularity) generally produces a bowel movement in 6 to 12 hours
Excerpt only. Read the full label for complete information.
About NDC 17856-1248
- What is NDC 17856-1248?
- 17856-1248 is the product NDC for Stimulant Laxative Plus Stool Softener, Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 tablet, film coated, listed with the FDA by ATLANTIC BIOLOGICALS CORP.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Stimulant Laxative Plus Stool Softener (Docusate Sodium 50 mg and Sennosides 8.6 mg).
- What is the active ingredient?
- Sennosides, Docusate sodium.
- Who is the labeler?
- ATLANTIC BIOLOGICALS CORP., NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Stimulant Laxative Plus Stool Softener?
- 4 other product NDCs are listed under this name. See all Stimulant Laxative Plus Stool Softener NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Stimulant Laxative Plus Stool Softener products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Stimulant Laxative Plus Stool Softenerdocusate sodium and sennosides | Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 | Tablet, Film coatedOral | GOOD SENSE | 50804-304 | 50804-0304-10 |
| Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mg | Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals, Inc. | 68788-7674 | 68788-7674-0168788-7674-06 |
| Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mg | Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 | Tablet, Film coatedOral | RUGBY LABORATORIES | 0536-1248 | 00536-1248-0100536-1248-10 |
| Stimulant Laxative Plus Stool Softenerdocusate sodium 50 mg and sennosides 8.6 mg | Sennosides 8.6 mg/1; Docusate sodium 50 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2693 | 71335-2693-0171335-2693-0271335-2693-03+6 more |
Other NDCs under M
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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| Broncochem Maximum Cough Kidsdextromethorphan hbr-guaifenesin | Dextromethorphan hydrobromide 10 mg/15mL; Guaifenesin 100 mg/15mL | SyrupOral | LABORATORIO MAGNACHEM INTERNATIONAL SRL | 65131-180 |
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| Hand Sanitizerantiseptic gel | Alcohol 62 g/100g | GelTopical | HART Health | 50332-0094 |
| Tribioticbacitracin zinc, neomycin sulfate, polymyxin b sulfate | Bacitracin zinc 400 [iU]/g + 2 more ingredients | OintmentTopical | HART Health | 50332-0095 |
| Therastatcherry cough drops | Menthol 5.8 mg/1 | LozengeOral | HART Health | 50332-0137 |
| Aspirin | Aspirin 325 mg/1 | TabletOral | HART Health | 50332-0139 |
| CETAFEN COUGH and COLDacetaminophen, dextromethorphan hbr, phenylephrine hcl , guaifenesin, , | Guaifenesin 100 mg/1 + 3 more ingredients | Tablet, Film coatedOral | HART Health | 50332-0141 |
| Hand Sanitizer Solution 101benzalkonium chloride | Benzalkonium chloride 13 kg/100kg | LiquidTopical | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. | 50241-224 |
| Histaprindiphenhydramine | Diphenhydramine hydrochloride 25 mg/1 | TabletOral | NorMed | 50332-0150 |
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| Cetafenacetaminophen | Acetaminophen 325 mg/1 | TabletOral | HART Health | 50332-0148 |
| MG DermaClean | Benzalkonium chloride .13 g/100g | LiquidTopical | Morgan Gallacher Inc. | 50241-014 |
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| Cetirzacetirizine hcl | Cetirizine hydrochloride 10 mg/1 | TabletOral | HART Health | 50332-0154 |
| MG DermaSan | Benzalkonium chloride .1 g/100g | LiquidTopical | Morgan Gallacher Inc. | 50241-259 |
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