What is NDC 10733-412?

10733-412 is the product NDC for lumicain (aluminium chloride hexahydrate), Aluminum chloride 250 mg/g solution, listed with the FDA by Medical Products Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

lumicain (Aluminium Chloride Hexahydrate).

Medical Products Laboratories, Inc., NDC labeler code 10733. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for lumicain?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

lumicain NDC 10733-412 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)10733-412Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10733-0412Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
10733-412-60	10733041260	67 g in 1 BOTTLE (10733-412-60)Marketed from Sep 29, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): lumicain
Generic name (nonproprietary): aluminium chloride hexahydrate
Active ingredients: Aluminum chloride — 250 mg/g
Dosage form: Solution
Route: Topical
Labeler: Medical Products Laboratories, Inc.NDC labeler code 10733
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Sep 29, 2010
Listing expires: Dec 31, 2026
Identifiers: Product ID 10733-412_b725dd26-c793-51a4-e053-2a95a90a573dSPL ID b725dd26-c793-51a4-e053-2a95a90a573dSPL set ID 9fdcce3e-e4d4-41ae-8609-37987c12414eRxCUI 244613, 486109UNII 3CYT62D3GA

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N410733041260 followed by a unit qualifier and the quantity

Package 10733-0412-60. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 23, 2020.

Full label on DailyMed (opens in a new tab)

About NDC 10733-412

What is NDC 10733-412?: 10733-412 is the product NDC for lumicain (aluminium chloride hexahydrate), Aluminum chloride 250 mg/g solution, listed with the FDA by Medical Products Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: lumicain (Aluminium Chloride Hexahydrate).
What is the active ingredient?: Aluminum chloride.
Who is the labeler?: Medical Products Laboratories, Inc., NDC labeler code 10733. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for lumicain?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

lumicain (Aluminium chloride hexahydrate) NDC 10733-412