Candida albicans NDC 0220-1134

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-1134Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-1134Add 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
0220-1134-41	00220113441	30 [hp_C] in 1 TUBE (0220-1134-41)Marketed from Mar 3, 1983
0220-1134-43	00220113443	3 TUBE in 1 CARTON (0220-1134-43) / 30 [hp_C] in 1 TUBE (0220-1134-41)Marketed from Feb 1, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Candida albicans
Generic name (nonproprietary): candida albicans
Active ingredients: Candida albicans — 30 [hp_C]/30[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 0220-1134_500d84f9-674c-9c91-e063-6394a90a8b4bSPL ID 500d84f9-674c-9c91-e063-6394a90a8b4bSPL set ID 849deed5-95a3-c3d1-e053-2991aa0ad164UNII 4D7G21HDBC
Pharmacologic class: Non-Standardized Fungal 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

N400220113441 followed by a unit qualifier and the quantity

Package 00220-1134-41. 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 Apr 22, 2026.

Indications (excerpt from the label)

Uses* ▪ if this is the first time you have vaginal itching and discomfort, see your doctor to find out if you have a vaginal yeast infection ▪ temporarily relieves symptoms of vaginal yeast infection (candidiasis) such as: ▪ minor vaginal itching ▪ burning ▪ discharge ▪ discomfort

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)