What is NDC 61727-309?

61727-309 is the product NDC for Muscular Pain Relief, Arnica montana 18 [hp_X]/4g + 4 more ingredients pellet, listed with the FDA by Homeocare Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Muscular Pain Relief (Arnica montana, Copper, Potassium phosphate, Dibasic, Lactic acid, Dl-,Magnesium phosphate, Dibasic trihydrate).

What is the active ingredient?

Arnica montana, Copper, Potassium phosphate, Dibasic, Lactic acid, Dl-, Magnesium phosphate, Dibasic trihydrate.

Homeocare Laboratories, NDC labeler code 61727. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Muscular Pain Relief?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Muscular Pain Relief NDC 61727-309

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-309Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0309Add 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
61727-309-21	6172703092161727030921	4 g in 1 TUBE (61727-309-21)Marketed from Jul 23, 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): Muscular Pain Relief
Generic name (nonproprietary): arnica montana, copper, potassium phosphate, dibasic, lactic acid, dl-,magnesium phosphate, dibasic trihydrate
Active ingredients: Arnica montana — 18 [hp_X]/4gCopper — 10 [hp_X]/4gPotassium phosphate, Dibasic — 8 [hp_X]/4gLactic acid, Dl- — 8 [hp_X]/4gMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare LaboratoriesNDC labeler code 61727
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 23, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 61727-309_7df3be22-b168-52d5-e053-2a91aa0ab75bSPL ID 7df3be22-b168-52d5-e053-2a91aa0ab75bSPL set ID 7ef95005-8cd2-4d7d-af73-4d3dd47128dbUNII O80TY208ZW, 789U1901C5, CI71S98N1Z, 3B8D35Y7S4, HF539G9L3QUPC 0361727309211
Pharmacologic class: Calculi Dissolution Agent; Copper-containing Intrauterine Device; Osmotic Laxative

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

N461727030921 followed by a unit qualifier and the quantity

Package 61727-0309-21. 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 Dec 26, 2018.

Indications (excerpt from the label)

Indications & Usage: Turn tube 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)

About NDC 61727-309

What is NDC 61727-309?: 61727-309 is the product NDC for Muscular Pain Relief, Arnica montana 18 [hp_X]/4g + 4 more ingredients pellet, listed with the FDA by Homeocare Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Muscular Pain Relief (Arnica montana, Copper, Potassium phosphate, Dibasic, Lactic acid, Dl-,Magnesium phosphate, Dibasic trihydrate).
What is the active ingredient?: Arnica montana, Copper, Potassium phosphate, Dibasic, Lactic acid, Dl-, Magnesium phosphate, Dibasic trihydrate.
Who is the labeler?: Homeocare Laboratories, NDC labeler code 61727. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Muscular Pain Relief?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.