natural senna laxative
Generic: sennosides
Labeler: basic drugs, inc.Drug Facts
Product Profile
Brand Name
natural senna laxative
Generic Name
sennosides
Labeler
basic drugs, inc.
Dosage Form
TABLET
Routes
Active Ingredients
sennosides 8.6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0761-0790
Product ID
0761-0790_21e5a19b-f8b7-d14c-e063-6394a90a9f99
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2021-12-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07610790
Hyphenated Format
0761-0790
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
natural senna laxative (source: ndc)
Generic Name
sennosides (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8.6 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (0761-0790-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21e5a19b-f8b7-d14c-e063-6394a90a9f99", "openfda": {"unii": ["3FYP5M0IJX"], "rxcui": ["312935"], "spl_set_id": ["d32ab3e7-7942-7420-e053-2a95a90aa024"], "manufacturer_name": ["Basic Drugs, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0761-0790-02)", "package_ndc": "0761-0790-02", "marketing_start_date": "20211214"}], "brand_name": "NATURAL SENNA LAXATIVE", "product_id": "0761-0790_21e5a19b-f8b7-d14c-e063-6394a90a9f99", "dosage_form": "TABLET", "product_ndc": "0761-0790", "generic_name": "SENNOSIDES", "labeler_name": "Basic Drugs, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NATURAL SENNA LAXATIVE", "active_ingredients": [{"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}