EZ-Quit NDC 61727-324

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-324Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0324Add 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
61727-324-21	61727032421	4 g in 1 TUBE (61727-324-21)Marketed from Aug 1, 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): EZ-Quit
Generic name (nonproprietary): antimony trisulfide, dieffenbachia seguine, strychnos ignatii seed, lobelia inflata, tobacco leaf
Active ingredients: Antimony trisulfide — 5 [hp_C]/4gDieffenbachia seguine — 5 [hp_C]/4gStrychnos ignatii seed — 5 [hp_C]/4gLobelia inflata — 5 [hp_C]/4gStrychnos nux-vomica seed — 5 [hp_C]/4gTobacco leaf — 9 [hp_C]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 1, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 61727-324_7e58e649-2149-e929-e053-2991aa0a320bSPL ID 7e58e649-2149-e929-e053-2991aa0a320bSPL set ID 44dca828-04b2-4346-9094-17dea2dd8159UNII F79059A38U, 01800C6E6B, 1NM3M2487K, 9PP1T3TC5U, 269XH13919, 6YR2608RSUUPC 0361727324214
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

N461727032421 followed by a unit qualifier and the quantity

Package 61727-0324-21. 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 31, 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)