Constipation Cp NDC 43406-0057

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0057Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0057Add 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
43406-0057-1	43406005701	30 mL in 1 BOTTLE, DROPPER (43406-0057-1)Marketed from Jan 1, 2010

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 Cp
Generic name (nonproprietary): aluminum oxide, bryonia alba root, matricaria recutita, graphite, lycopodium clavatum spore, strychnos nux-vomica seed, silicon dioxide, sulfur, sodium chloride, magnesium chloride, lead, sepia officinalis juice.
Active ingredients: Aluminum oxide — 30 [hp_C]/mLBryonia alba root — 30 [hp_C]/mLMatricaria recutita — 30 [hp_C]/mLGraphite — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLSulfur — 30 [hp_C]/mLSodium chloride — 30 [hp_C]/mLMagnesium chloride — 30 [hp_C]/mLLead — 30 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (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)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43406-0057_384d29dc-dfcd-445d-acf8-d00397950a18SPL ID 384d29dc-dfcd-445d-acf8-d00397950a18SPL set ID 961b3ddf-41fe-46ed-b5e4-0fd8d9652edfUNII LMI26O6933, T7J046YI2B, G0R4UBI2ZZ, 4QQN74LH4O, C88X29Y479, 269XH13919, ETJ7Z6XBU4, 70FD1KFU70, 451W47IQ8X, 02F3473H9O, 2P299V784P, QDL83WN8C2UPC 0877730001023
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

N443406005701 followed by a unit qualifier and the quantity

Package 43406-0057-01. 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 15, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves infrequent bowel movements, difficult passage of stool &/or other symptoms of constipation.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)