natural laxative
Generic: sennosides 8.6 mg
Labeler: bi-martDrug Facts
Product Profile
Brand Name
natural laxative
Generic Name
sennosides 8.6 mg
Labeler
bi-mart
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sennosides 8.6 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37835-211
Product ID
37835-211_40ca4164-3b27-bc2a-e063-6294a90a35cb
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2025-07-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37835211
Hyphenated Format
37835-211
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 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
- 100 TABLET, FILM COATED in 1 BOTTLE (37835-211-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40ca4164-3b27-bc2a-e063-6294a90a35cb", "openfda": {"unii": ["3FYP5M0IJX"], "rxcui": ["312935"], "spl_set_id": ["af36e020-0e6f-40b3-b521-25b60e324116"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (37835-211-01)", "package_ndc": "37835-211-01", "marketing_start_date": "20250701"}], "brand_name": "Natural Laxative", "product_id": "37835-211_40ca4164-3b27-bc2a-e063-6294a90a35cb", "dosage_form": "TABLET, FILM COATED", "product_ndc": "37835-211", "generic_name": "Sennosides 8.6 mg", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Natural Laxative", "active_ingredients": [{"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}