sennosides and docusate sodium

Generic: sennosides and docusate sodium

Labeler: american health packaging
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sennosides and docusate sodium
Generic Name sennosides and docusate sodium
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/1, sennosides 8.6 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-622
Product ID 60687-622_3c2f58eb-5f46-5945-e063-6294a90a40c0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2021-08-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687622
Hyphenated Format 60687-622

Supplemental Identifiers

RxCUI
998740
UNII
F05Q2T2JA0 3FYP5M0IJX

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sennosides and docusate sodium (source: ndc)
Generic Name sennosides and docusate sodium (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-622-01) / 1 TABLET in 1 BLISTER PACK (60687-622-11)
source: ndc

Packages (1)

Ingredients (2)

docusate sodium (50 mg/1) sennosides (8.6 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c2f58eb-5f46-5945-e063-6294a90a40c0", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["4b84d5d7-43cf-47bb-af59-088550c3a0bc"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-622-01)  / 1 TABLET in 1 BLISTER PACK (60687-622-11)", "package_ndc": "60687-622-01", "marketing_start_date": "20210803"}], "brand_name": "Sennosides and Docusate Sodium", "product_id": "60687-622_3c2f58eb-5f46-5945-e063-6294a90a40c0", "dosage_form": "TABLET", "product_ndc": "60687-622", "generic_name": "Sennosides and Docusate Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sennosides and Docusate Sodium", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210803", "listing_expiration_date": "20261231"}