Constipation NDC 55714-2413

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2413Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2413Add 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
55714-2413-1	55714241301	28 g in 1 BOTTLE, GLASS (55714-2413-1)Marketed from Jan 31, 2019

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): Constipation
Generic name (nonproprietary): abies nig., aesculus hipp., aloe, alumina, bryonia, carbo veg., chelidonium majus, collinsonia , graphites, hydrastis, kali carb., lycopodium, mag. mur., mezereum, nux vom., podoph. pelt., rhamnus purshiana, sanicula, selenium, sepia, silicea, tabacum, veratrum alb., zinc.met., echinacea, iris versicolor, phytolacca, taraxacum
Active ingredients: Picea mariana resin — 15 [hp_X]/gHorse chestnut — 15 [hp_X]/gAloe — 15 [hp_X]/gAluminum oxide — 15 [hp_X]/gBryonia alba root — 15 [hp_X]/gActivated charcoal — 15 [hp_X]/gChelidonium majus — 15 [hp_X]/gCollinsonia canadensis root — 15 [hp_X]/gGraphite — 15 [hp_X]/gGoldenseal — 15 [hp_X]/gPotassium carbonate — 15 [hp_X]/gLycopodium clavatum spore — 15 [hp_X]/gMagnesium chloride — 15 [hp_X]/gDaphne mezereum bark — 15 [hp_X]/gStrychnos nux-vomica seed — 15 [hp_X]/gPodophyllum — 15 [hp_X]/gFrangula purshiana bark — 15 [hp_X]/gSanicula europaea leaf — 15 [hp_X]/gSelenium — 15 [hp_X]/gSepia officinalis juice — 15 [hp_X]/gSilicon dioxide — 15 [hp_X]/gTobacco leaf — 15 [hp_X]/gVeratrum album root — 15 [hp_X]/gZinc — 15 [hp_X]/gEchinacea, Unspecified — 6 [hp_X]/gIris versicolor root — 6 [hp_X]/gPhytolacca americana root — 6 [hp_X]/gTaraxacum officinale — 6 [hp_X]/g
Dosage form: Pellet
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 31, 2019
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)Increased Large Intestinal Motility (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)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 55714-2413_b4e15f8c-3af7-71fe-e053-2a95a90a003eSPL ID b4e15f8c-3af7-71fe-e053-2a95a90a003eSPL set ID 90804a94-1e67-3ab3-e053-2a95a90aafbeUNII 71AOV0W131, 3C18L6RJAZ, V5VD430YW9, LMI26O6933, T7J046YI2B, 2P3VWU3H10, 7E889U5RNN, O2630F3XDR, 4QQN74LH4O, ZW3Z11D0JV, BQN1B9B9HA, C88X29Y479, 02F3473H9O, X2N6E405GV, 269XH13919, 2S713A4VP3, 4VBP01X99F, JYZ6110L9I, H6241UJ22B, QDL83WN8C2, ETJ7Z6XBU4, 6YR2608RSU, QNS6W5US1Z, J41CSQ7QDS, 4N9P6CC1DX, X43D4L3DQC, 11E6VI8VEG, 39981FM375
Pharmacologic class: Calculi Dissolution Agent; Non-Standardized Plant Allergenic Extract; 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N455714241301 followed by a unit qualifier and the quantity

Package 55714-2413-01. 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 Nov 24, 2020.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as difficult elimination, hard stools, pain, cramping, itching and bloating.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)