Equate Yeast Relief NDC 79903-094

NDC codes

FDA NDC Directory

Product NDC (as listed)79903-094Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79903-0094Add 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
79903-094-14	79903009414	60 BLISTER PACK in 1 BOX (79903-094-14) / 1 TABLET in 1 BLISTER PACKMarketed from Mar 4, 2022

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): Equate Yeast Relief
Generic name (nonproprietary): candida albicans, wood creosote, sodium chloride, and sulfur
Active ingredients: Candida albicans — 30 [hp_X]/1Wood creosote — 30 [hp_X]/1Sodium chloride — 12 [hp_X]/1Sulfur — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: WAL-MART STORES INC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 4, 2022
Listing expires: Dec 31, 2026
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 79903-094_462e764a-7083-ddae-e063-6394a90a925dSPL ID 462e764a-7083-ddae-e063-6394a90a925dSPL set ID d96aa608-ed8a-36cd-e053-2a95a90ac286UNII 4D7G21HDBC, 3JYG22FD73, 451W47IQ8X, 70FD1KFU70UPC 0681131449076
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

N479903009414 followed by a unit qualifier and the quantity

Package 79903-0094-14. 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 Dec 17, 2025.

Indications (excerpt from the label)

Uses See your doctor if this is the first time you have vaginal itching and discomfort to find out if you have a vaginal yeast infection. According to homeopathic indications, these ingredients provide temporary relief of yeast infection related symprtoms such as: itching and burning, occasional vaginal odor and discharge, after consultation by a physician. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

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