BHI Constipation NDC 62795-1005

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1005Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1005Add 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
62795-1005-3	62795100503	1 BOTTLE in 1 CARTON (62795-1005-3) / 100 TABLET in 1 BOTTLEMarketed from Aug 30, 2014

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): BHI Constipation
Generic name (nonproprietary): dioscorea villosa tuber, sodium chloride, and strychnos nux-vomica seed
Active ingredients: Dioscorea villosa tuber — 4 [hp_X]/1Sodium chloride — 200 [hp_X]/1Strychnos nux-vomica seed — 8 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: MediNatura Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 30, 2014
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)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 62795-1005_25f16472-f472-48be-a1f9-d5741bcf2686SPL ID 25f16472-f472-48be-a1f9-d5741bcf2686SPL set ID 0365b75b-fee4-4c1d-89ab-c692bdd73f75UNII IWY3IWX2G8, 451W47IQ8X, 269XH13919
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462795100503 followed by a unit qualifier and the quantity

Package 62795-1005-03. 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 Jul 7, 2022.

Indications (excerpt from the label)

USES For the temporary relief of minor constipation, bowel irregularity, bloating

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)