Aluminum Muriaticum NDC 37662-2703

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-2703Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-2703Add 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
37662-2703-1	37662270301	200 PELLET in 1 VIAL, GLASS (37662-2703-1)Marketed from Feb 23, 2023
37662-2703-2	37662270302	1200 PELLET in 1 BOTTLE, GLASS (37662-2703-2)Marketed from Feb 23, 2023
37662-2703-3	37662270303	4000 PELLET in 1 BOTTLE, GLASS (37662-2703-3)Marketed from Feb 23, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Aluminum Muriaticum
Generic name (nonproprietary): aluminum muriaticum
Active ingredients: Aluminum chloride anhydrous — 12 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 23, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 37662-2703_f56a0700-4416-2dbb-e053-2995a90a3a03SPL ID f56a0700-4416-2dbb-e053-2995a90a3a03SPL set ID f56a0700-4415-2dbb-e053-2995a90a3a03UNII LIF1N9568Y

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N437662270301 followed by a unit qualifier and the quantity

Package 37662-2703-01. 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 Feb 23, 2023.

Full label on DailyMed (opens in a new tab)