Headache Relief NDC 61727-305

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-305Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0305Add 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
61727-305-21	61727030521	4 g in 1 TUBE (61727-305-21)Marketed from Jul 20, 2012

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): Headache Relief
Generic name (nonproprietary): atropa belladonna, cyclamen purpurascens tuber, coffea arabica seed, roasted, iris versicolor root, strychnos nux-vomica seed, sanguinaria canadensis root, spigelia marilandica root, viburnum opulus bark
Active ingredients: Atropa belladonna — 8 [hp_C]/4gCyclamen purpurascens tuber — 8 [hp_C]/4gCoffea arabica seed, Roasted — 4 [hp_C]/4gIris versicolor root — 8 [hp_C]/4gStrychnos nux-vomica seed — 9 [hp_C]/4gSanguinaria canadensis root — 8 [hp_C]/4gSpigelia marilandica root — 8 [hp_C]/4gViburnum opulus bark — 4 [hp_C]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 61727-305_483751f9-ce23-d744-e063-6294a90a7b3fSPL ID 483751f9-ce23-d744-e063-6294a90a7b3fSPL set ID 47f7bcbc-f4be-4cf0-a5b0-b8d5ca8d852fUNII WQZ3G9PF0H, G728143D8Q, 9H58JRT35E, X43D4L3DQC, 269XH13919, N9288CD508, 467D26HS0B, T1UG6H6805UPC 0361727305213
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

NDC on a medical claim

N461727030521 followed by a unit qualifier and the quantity

Package 61727-0305-21. 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 12, 2026.

Indications (excerpt from the label)

Indications & Usage: Turn turn upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)