Package 10733-412-60

Brand: lumicain

Generic: aluminium chloride hexahydrate
NDC Package

Package Facts

Identity

Package NDC 10733-412-60
Digits Only 1073341260
Product NDC 10733-412
Product ID 10733-412_b725dd26-c793-51a4-e053-2a95a90a573d
Description

67 g in 1 BOTTLE (10733-412-60)

Marketing

Marketing Status
Marketed Since 2020-09-29
Brand lumicain
Generic aluminium chloride hexahydrate
Sample Package No

Linked Drug Pages (1)

lumicain ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "b725dd26-c793-51a4-e053-2a95a90a573d", "openfda": {"unii": ["3CYT62D3GA"], "rxcui": ["244613", "486109"], "spl_set_id": ["9fdcce3e-e4d4-41ae-8609-37987c12414e"], "manufacturer_name": ["Medical Products Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "67 g in 1 BOTTLE (10733-412-60)", "package_ndc": "10733-412-60", "marketing_start_date": "20200929"}], "brand_name": "lumicain", "product_id": "10733-412_b725dd26-c793-51a4-e053-2a95a90a573d", "dosage_form": "SOLUTION", "product_ndc": "10733-412", "generic_name": "Aluminium Chloride Hexahydrate", "labeler_name": "Medical Products Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lumicain", "active_ingredients": [{"name": "ALUMINUM CHLORIDE", "strength": "250 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20100929", "listing_expiration_date": "20261231"}