Ring HP NDC 44911-0626

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0626Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0626Add 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
44911-0626-1	44911062601	30 mL in 1 BOTTLE, DROPPER (44911-0626-1)Marketed from Dec 21, 2020

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): Ring HP
Generic name (nonproprietary): ginkgo biloba, chininum sulphuricum, cinchona officinalis, graphites, natrum salicylicum, plumbum metallicum, salicylicum acidum, spigelia anthelmia, thiosinaminum
Active ingredients: Ginkgo — 6 [hp_X]/mLQuinine sulfate — 30 [hp_X]/mLCinchona officinalis bark — 30 [hp_X]/mLGraphite — 30 [hp_X]/mLSodium salicylate — 30 [hp_X]/mLLead — 30 [hp_X]/mLSalicylic acid — 30 [hp_X]/mLSpigelia anthelmia whole — 30 [hp_X]/mLAllylthiourea — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 21, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0626_dfb88b6d-ce5b-4ee0-9fca-6a7946664679SPL ID dfb88b6d-ce5b-4ee0-9fca-6a7946664679SPL set ID 7a33d174-f8e3-433d-9f8d-4d1db1325d1fUNII 19FUJ2C58T, KF7Z0E0Q2B, S003A158SB, 4QQN74LH4O, WIQ1H85SYP, 2P299V784P, O414PZ4LPZ, WYT05213GE, 706IDJ14B7UPC 0363113700886
Pharmacologic class: Antimalarial

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

N444911062601 followed by a unit qualifier and the quantity

Package 44911-0626-01. 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 Aug 22, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporary relief noises of the ears, such as ringing, buzzing, roaring.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)