Constipation Relief NDC 61727-304

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-304Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0304Add 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
61727-304-21	61727030421	4 g in 1 TUBE (61727-304-21)Marketed from Jul 5, 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): Constipation Relief
Generic name (nonproprietary): aluminum oxide, bryonia alba root, sodium chloride, graphite, silicon dioxide
Active ingredients: Aluminum oxide — 10 [hp_X]/4gBryonia alba root — 8 [hp_X]/4gSodium chloride — 8 [hp_X]/4gGraphite — 10 [hp_X]/4gSilicon dioxide — 10 [hp_X]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 5, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers: Product ID 61727-304_4836c0cb-504d-e24b-e063-6294a90a4e31SPL ID 4836c0cb-504d-e24b-e063-6294a90a4e31SPL set ID 62374240-cd14-44e2-9405-5f8996faf047UNII LMI26O6933, T7J046YI2B, 451W47IQ8X, 4QQN74LH4O, ETJ7Z6XBU4UPC 0361727304216
Pharmacologic class: 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

N461727030421 followed by a unit qualifier and the quantity

Package 61727-0304-21. 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 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)