Package 82714-001-01

Brand: bluestop max

Generic: external analgesic
NDC Package

Package Facts

Identity

Package NDC 82714-001-01
Digits Only 8271400101
Product NDC 82714-001
Product ID 82714-001_4835cc39-0fd2-f27e-e063-6294a90abf4f
Description

1 APPLICATOR in 1 CARTON (82714-001-01) / 85 g in 1 APPLICATOR

Marketing

Marketing Status
Marketed Since 2023-01-10
Brand bluestop max
Generic external analgesic
Sample Package No

Linked Drug Pages (1)

BlueStop Max ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4835cc39-0fd2-f27e-e063-6294a90abf4f", "openfda": {"upc": ["0832492046835"], "unii": ["V13007Z41A", "L7T10EIP3A"], "rxcui": ["1373137"], "spl_set_id": ["f1efb51c-5217-4cb2-e053-2a95a90a7f95"], "manufacturer_name": ["Clavel Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (82714-001-01)  / 85 g in 1 APPLICATOR", "package_ndc": "82714-001-01", "marketing_start_date": "20230110"}], "brand_name": "BlueStop Max", "product_id": "82714-001_4835cc39-0fd2-f27e-e063-6294a90abf4f", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "82714-001", "generic_name": "External Analgesic", "labeler_name": "Clavel Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BlueStop Max", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/g"}, {"name": "MENTHOL", "strength": "10 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230110", "listing_expiration_date": "20271231"}