Package 53675-212-00

Brand: aruba aloe alcoholada

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53675-212-00
Digits Only 5367521200
Product NDC 53675-212
Description

251 mL in 1 TUBE (53675-212-00)

Marketing

Marketing Status
Marketed Since 2025-06-15
Brand aruba aloe alcoholada
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3bc81f57-d185-ecb6-e063-6394a90a29e3", "openfda": {"upc": ["0082252031209"], "unii": ["V13007Z41A"], "spl_set_id": ["f56c62b0-75db-4499-858e-54e10b0e140a"], "manufacturer_name": ["Aruba Aloe Balm NV"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "251 mL in 1 TUBE (53675-212-00)", "package_ndc": "53675-212-00", "marketing_start_date": "20250615"}], "brand_name": "Aruba Aloe Alcoholada", "product_id": "53675-212_3bc81f57-d185-ecb6-e063-6394a90a29e3", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "53675-212", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Aruba Aloe Balm NV", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aruba Aloe Alcoholada", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250615", "listing_expiration_date": "20261231"}