senna laxative
Generic: sennosides 8.6 mg
Labeler: nuvicare llcDrug Facts
Product Profile
Brand Name
senna laxative
Generic Name
sennosides 8.6 mg
Labeler
nuvicare llc
Dosage Form
TABLET
Routes
Active Ingredients
sennosides 8.6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
84324-012
Product ID
84324-012_bfbd8b84-7865-457a-9693-c2b2fef5411b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2024-07-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84324012
Hyphenated Format
84324-012
Supplemental Identifiers
RxCUI
UPC
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 laxative (source: ndc)
Generic Name
sennosides 8.6 mg (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.6 mg/1
Packaging
- 200 TABLET in 1 BOTTLE (84324-012-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bfbd8b84-7865-457a-9693-c2b2fef5411b", "openfda": {"upc": ["0384324000107"], "unii": ["3FYP5M0IJX"], "rxcui": ["312935"], "spl_set_id": ["372e8b67-2b9a-4416-b6c2-f44fd24f35e9"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (84324-012-01)", "package_ndc": "84324-012-01", "marketing_start_date": "20240717"}], "brand_name": "Senna Laxative", "product_id": "84324-012_bfbd8b84-7865-457a-9693-c2b2fef5411b", "dosage_form": "TABLET", "product_ndc": "84324-012", "generic_name": "Sennosides 8.6 mg", "labeler_name": "NUVICARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Senna Laxative", "active_ingredients": [{"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240717", "listing_expiration_date": "20261231"}