Package 14448-306-40
Brand: super white stuff pain relief
Generic: mentholPackage Facts
Identity
Package NDC
14448-306-40
Digits Only
1444830640
Product NDC
14448-306
Description
130 mL in 1 JAR (14448-306-40)
Marketing
Marketing Status
Brand
super white stuff pain relief
Generic
menthol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09d6fabb-0d18-222e-e063-6294a90a95b6", "openfda": {"upc": ["0673314002888"], "unii": ["L7T10EIP3A"], "rxcui": ["2391332"], "spl_set_id": ["9f948fb4-4275-4a1f-83f8-cd708db4a296"], "manufacturer_name": ["BLUE SPRING WELLNESS, L.L.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "130 mL in 1 JAR (14448-306-40)", "package_ndc": "14448-306-40", "marketing_start_date": "20200801"}], "brand_name": "SUPER WHITE STUFF Pain Relief", "product_id": "14448-306_09d6fabb-0d18-222e-e063-6294a90a95b6", "dosage_form": "CREAM", "product_ndc": "14448-306", "generic_name": "MENTHOL", "labeler_name": "BLUE SPRING WELLNESS, L.L.C.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUPER WHITE STUFF Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "14 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}