Over-the-counter drug · OTC MONOGRAPH DRUG
Stool Softener plus Laxative NDC 63868-878
docusate sodium, sennosides · Docusate sodium 50 mg/1; Sennosides 8.6 mg/1 · Tablet · Oral · QUALITY CHOICE (Chain Drug Marketing Association)
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63868-878-60 | 63868087860 | 1 BOTTLE in 1 BOX (63868-878-60) / 60 TABLET in 1 BOTTLEMarketed from Oct 30, 2019 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Stool Softener plus Laxative
- Generic name (nonproprietary)
- docusate sodium, sennosides
- Active ingredients
- Docusate sodium — 50 mg/1Sennosides — 8.6 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 63868-878_a8f763b4-933f-4710-9dcd-3ef62de4432fSPL ID a8f763b4-933f-4710-9dcd-3ef62de4432fSPL set ID ebb35e67-4e83-445e-af6e-ecb43b1d3df6RxCUI 998740UNII F05Q2T2JA0, 3FYP5M0IJXUPC 0635515997158
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
N463868087860followed by a unit qualifier and the quantityPackage 63868-0878-60. 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 causes bowel movement in 6- 12 hours.
Excerpt only. Read the full label for complete information.
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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| Antibacterial Foaming Skin Cleanserbenzalkonium chloride | Benzalkonium chloride .13 mg/mL | SoapTopical | Betco Corporation, Ltd. | 65601-709 |
| Hawthorn Hygiene Solutions ENERGY ANTIBACTERIAL FOAM FRAGRANCE FREE 1200 mLbenzalkonium chloride | Benzalkonium chloride .0013 mg/mL | LiquidTopical | BUNZL Distribution | 66294-114 |
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| Fresh Feels Hand Sanitizer Mist Seashell Sunshine Scentethyl alcohol | Alcohol 70 mL/100mL | SprayTopical | Amber Glow Cosmetics Limited | 87302-202 |
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| Safeguard Antibacterial Foamingbenzalkonium chloride | Benzalkonium chloride .12 g/100mL | SoapTopical | The Procter & Gamble Manufacturing Company | 37000-601 |
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