Package 14448-307-50

Brand: super white stuff pain relief

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 14448-307-50
Digits Only 1444830750
Product NDC 14448-307
Description

335 mL in 1 BOTTLE (14448-307-50)

Marketing

Marketing Status
Marketed Since 2020-08-01
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": "09d7052e-ec52-ef60-e063-6294a90af214", "openfda": {"upc": ["0673314002895"], "unii": ["L7T10EIP3A"], "rxcui": ["2391332"], "spl_set_id": ["7779b26b-ae3b-4639-a6b0-826c7ab37a86"], "manufacturer_name": ["BLUE SPRING WELLNESS, L.L.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "335 mL in 1 BOTTLE (14448-307-50)", "package_ndc": "14448-307-50", "marketing_start_date": "20200801"}], "brand_name": "SUPER WHITE Stuff Pain Relief", "product_id": "14448-307_09d7052e-ec52-ef60-e063-6294a90af214", "dosage_form": "CREAM", "product_ndc": "14448-307", "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"}