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SENNA-S

NDC 69517-131, Senna and Docusate Sodium Tablets, 8.6 mg and 50 mg, tablet, coated, from HealthLife of USA LLC.

Product NDC
69517-131
Status
Listed
Labeler
HealthLife of USA LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
505G(a)(3)
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69517-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SENNOSIDES8.6 mg/1
  • DOCUSATE SODIUM50 mg/1
Package NDCNDC-11Package
69517-131-02695170131022 POUCH in 1 POUCH (69517-131-02) / 2 TABLET, COATED in 1 POUCH
69517-131-10695170131101000 BOTTLE in 1 BOTTLE (69517-131-10) / 500 BOTTLE in 1 BOTTLE (69517-131-05) / 24 CARTON in 1 BOTTLE (69517-131-24) / 1 TABLET, COATED in 1 CARTON
69517-131-256951701312525 POUCH in 1 BOX (69517-131-25) / 2 TABLET, COATED in 1 POUCH
69517-131-506951701315050 POUCH in 1 BOX (69517-131-50) / 2 TABLET, COATED in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 69517-131 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69517-131 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69517-131. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.