Earache Relief NDC 43689-0020

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0020Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0020Add 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
43689-0020-2	43689002002	1 BOTTLE in 1 PACKAGE (43689-0020-2) / 90 TABLET in 1 BOTTLE (43689-0020-1)Marketed from Aug 24, 2016

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): Earache Relief
Generic name (nonproprietary): belladonna, calcarea carbonica, chamomilla, hepar sulphuris calcareum, kali bichromicum, lycopodium clavatum, plantago major, pulsatilla (vulgaris)
Active ingredients: Atropa belladonna — 12 [hp_X]/1Oyster shell calcium carbonate, Crude — 12 [hp_X]/1Matricaria chamomilla whole — 12 [hp_X]/1Calcium sulfide — 12 [hp_X]/1Potassium dichromate — 12 [hp_X]/1Lycopodium clavatum spore — 12 [hp_X]/1Plantago major whole — 12 [hp_X]/1Pulsatilla vulgaris whole — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: The Magni Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 9, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 43689-0020_32934d7c-c3dc-4bfc-8b8c-ffbbc39768deSPL ID 32934d7c-c3dc-4bfc-8b8c-ffbbc39768deSPL set ID 3f62001a-27b5-43cb-8006-110943facf87UNII WQZ3G9PF0H, 2E32821G6I, G0R4UBI2ZZ, 1MBW07J51Q, T4423S18FM, C88X29Y479, W2469WNO6U, I76KB35JEV

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

N443689002002 followed by a unit qualifier and the quantity

Package 43689-0020-02. 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 Nov 5, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of earache symptoms, such as pain, pressure, congestion, itching, sleeplessness, and headaches, after diagnosis by a physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)