lumicain

Generic: aluminium chloride hexahydrate

Labeler: medical products laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name lumicain
Generic Name aluminium chloride hexahydrate
Labeler medical products laboratories, inc.
Dosage Form SOLUTION
Routes
TOPICAL
Active Ingredients

aluminum chloride 250 mg/g

Manufacturer
Medical Products Laboratories, Inc.

Identifiers & Regulatory

Product NDC 10733-412
Product ID 10733-412_b725dd26-c793-51a4-e053-2a95a90a573d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2010-09-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10733412
Hyphenated Format 10733-412

Supplemental Identifiers

RxCUI
244613 486109
UNII
3CYT62D3GA

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lumicain (source: ndc)
Generic Name aluminium chloride hexahydrate (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/g
source: ndc
Packaging
  • 67 g in 1 BOTTLE (10733-412-60)
source: ndc

Packages (1)

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

Ingredients (1)

aluminum chloride (250 mg/g)

Linked Drug Pages (1)

lumicain ndc-match (0.9)

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"}