What is NDC 68400-203?

68400-203 is the product NDC for Hemox A (aluminum chloride), Aluminum chloride 7500 mg/30mL solution, listed with the FDA by Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc., NDC labeler code 68400. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hemox A?

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.

Hemox A NDC 68400-203 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68400-203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68400-0203Add 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
68400-203-18	6840002031868400020318	30 mL in 1 BOTTLE, GLASS (68400-203-18)Marketed from Oct 1, 2018

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): Hemox A
Generic name (nonproprietary): aluminum chloride
Active ingredients: Aluminum chloride — 7500 mg/30mL
Dosage form: Solution
Route: Dental
Labeler: Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.NDC labeler code 68400
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 15, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 68400-203_d6095e73-2eed-5f18-e053-2995a90abe8fSPL ID d6095e73-2eed-5f18-e053-2995a90abe8fSPL set ID cf98eb6f-c16e-4541-9d3e-bfaa3a4a5ff2RxCUI 244613, 672193UNII 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N468400020318 followed by a unit qualifier and the quantity

Package 68400-0203-18. 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 Jan 20, 2022.

Full label on DailyMed (opens in a new tab)

About NDC 68400-203

What is NDC 68400-203?: 68400-203 is the product NDC for Hemox A (aluminum chloride), Aluminum chloride 7500 mg/30mL solution, listed with the FDA by Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hemox A (Aluminum Chloride).
What is the active ingredient?: Aluminum chloride.
Who is the labeler?: Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc., NDC labeler code 68400. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hemox A?: 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.

Hemox A (Aluminum chloride) NDC 68400-203