NDC 10733-412

lumicain

Aluminium Chloride Hexahydrate

lumicain is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Medical Products Laboratories, Inc.. The primary component is Aluminum Chloride.

• Product ID: 10733-412_13a2ec4c-8915-4875-a1ef-24395b846eda
• NDC: 10733-412
• Product Type: Human Prescription Drug
• Proprietary Name: lumicain
• Generic Name: Aluminium Chloride Hexahydrate
• Dosage Form: Solution
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-09-29
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Medical Products Laboratories, Inc.
• Substance Name: ALUMINUM CHLORIDE
• Active Ingredient Strength: 250 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10733-412-60

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

• Marketing Start Date: 2020-09-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10733-412-60 [10733041260]

lumicain SOLUTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-09-29
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
ALUMINUM CHLORIDE	250 mg/g

OpenFDA Data

• SPL SET ID: 9fdcce3e-e4d4-41ae-8609-37987c12414e
• Manufacturer:
  • Medical Products Laboratories, Inc.
• UNII:
  • 3CYT62D3GA
• RxNorm Concept Unique ID - RxCUI:
  • 486109
  • 244613