gurunanda sensitive
Generic: potassium nitrate
Labeler: gurunanda, llcDrug Facts
Product Profile
Brand Name
gurunanda sensitive
Generic Name
potassium nitrate
Labeler
gurunanda, llc
Dosage Form
PASTE
Routes
Active Ingredients
potassium nitrate 50 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
70708-645
Product ID
70708-645_48c6bb82-9696-0ed0-e063-6294a90a11a4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M022
Listing Expiration
2027-12-31
Marketing Start
2025-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70708645
Hyphenated Format
70708-645
Supplemental Identifiers
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
gurunanda sensitive (source: ndc)
Generic Name
potassium nitrate (source: ndc)
Application Number
M022 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/g
Packaging
- 1 TUBE in 1 CARTON (70708-645-04) / 119 g in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c6bb82-9696-0ed0-e063-6294a90a11a4", "openfda": {"unii": ["RU45X2JN0Z"], "spl_set_id": ["3ef0d3d4-fd42-0181-e063-6394a90af09c"], "manufacturer_name": ["GURUNANDA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70708-645-04) / 119 g in 1 TUBE", "package_ndc": "70708-645-04", "marketing_start_date": "20250926"}], "brand_name": "GuruNanda Sensitive", "product_id": "70708-645_48c6bb82-9696-0ed0-e063-6294a90a11a4", "dosage_form": "PASTE", "product_ndc": "70708-645", "generic_name": "Potassium Nitrate", "labeler_name": "GURUNANDA, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GuruNanda Sensitive", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20271231"}