senna syrup
Generic: sennosides
Labeler: pioneer life sciences, llcDrug Facts
Product Profile
Brand Name
senna syrup
Generic Name
sennosides
Labeler
pioneer life sciences, llc
Dosage Form
SYRUP
Routes
Active Ingredients
sennosides 8.8 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
72090-022
Product ID
72090-022_ac89faa4-0f3e-46e5-b01c-4c3920a3923f
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2024-10-18
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72090022
Hyphenated Format
72090-022
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
senna syrup (source: ndc)
Generic Name
sennosides (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.8 mg/5mL
Packaging
- 237 mL in 1 BOTTLE (72090-022-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ac89faa4-0f3e-46e5-b01c-4c3920a3923f", "openfda": {"unii": ["3FYP5M0IJX"], "rxcui": ["702311"], "spl_set_id": ["206d52bf-8982-4668-b750-b4e4d3c5dc66"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (72090-022-01)", "package_ndc": "72090-022-01", "marketing_start_date": "20241018"}], "brand_name": "Senna Syrup", "product_id": "72090-022_ac89faa4-0f3e-46e5-b01c-4c3920a3923f", "dosage_form": "SYRUP", "product_ndc": "72090-022", "generic_name": "SENNOSIDES", "labeler_name": "Pioneer Life Sciences, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senna Syrup", "active_ingredients": [{"name": "SENNOSIDES", "strength": "8.8 mg/5mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241018", "listing_expiration_date": "20261231"}