Pain Relief NDC 61626-0099

NDC codes

FDA NDC Directory

Product NDC (as listed)61626-0099Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61626-0099Add 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
61626-0099-4	61626009904	59 mL in 1 BOTTLE (61626-0099-4)Marketed from Dec 4, 2018

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): Pain Relief
Generic name (nonproprietary): arnica, chamomilla, hypericum, ignatia, symphytum
Active ingredients: Arnica montana — 12 [hp_X]/59mLMatricaria chamomilla — 12 [hp_X]/59mLHypericum perforatum — 12 [hp_X]/59mLStrychnos ignatii seed — 12 [hp_X]/59mLComfrey root — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: NET Remedies
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 4, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 61626-0099_b9492b5a-9070-4f3c-e053-2a95a90a6650SPL ID b9492b5a-9070-4f3c-e053-2a95a90a6650SPL set ID 75786c15-be49-4548-8f7a-319f86aa0ceeUNII O80TY208ZW, G0R4UBI2ZZ, XK4IUX8MNB, 1NM3M2487K, M9VVZ08EKQ

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

N461626009904 followed by a unit qualifier and the quantity

Package 61626-0099-04. 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 19, 2021.

Indications (excerpt from the label)

INDICATIONS FOR USE: For the temporary relief of general pain, includingm symptoms related to joints, bones, muscles, minor bruises, spinal pain and pain due to arthiritis. **

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)