Package 83591-629-00

Brand: bluespring doctors pain formula pain relief

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 83591-629-00
Digits Only 8359162900
Product NDC 83591-629
Description

355 mL in 1 JAR (83591-629-00)

Marketing

Marketing Status
Marketed Since 2025-07-07
Brand bluespring doctors pain formula 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": "39e0ad70-7af0-cd09-e063-6394a90a0f22", "openfda": {"upc": ["0673314003892"], "unii": ["L7T10EIP3A"], "rxcui": ["2391332"], "spl_set_id": ["98f3f719-792f-4a93-95b1-90072e0f8bf4"], "manufacturer_name": ["ACA MANAGEMENT LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 JAR (83591-629-00)", "package_ndc": "83591-629-00", "marketing_start_date": "20250707"}], "brand_name": "BLUESPRING Doctors Pain Formula Pain Relief", "product_id": "83591-629_39e0ad70-7af0-cd09-e063-6394a90a0f22", "dosage_form": "CREAM", "product_ndc": "83591-629", "generic_name": "MENTHOL", "labeler_name": "ACA MANAGEMENT LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BLUESPRING Doctors Pain Formula Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "14 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250707", "listing_expiration_date": "20261231"}