What is NDC 83004-011?

83004-011 is the product NDC for Anti Fungal Foot and Body, Sepia officinalis juice 12 [hp_X]/mL; Tea tree oil .04 g/mL liquid, listed with the FDA by Rida LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Anti Fungal Foot and Body (SEPIA OFFICINALIS JUICE,melaleuca alternifolia).

What is the active ingredient?

Sepia officinalis juice, Tea tree oil.

Rida LLC, NDC labeler code 83004. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Anti Fungal Foot and Body?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Anti Fungal Foot and Body NDC 83004-011

NDC codes

FDA NDC Directory

Product NDC (as listed)83004-011Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83004-0011Add 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
83004-011-01	83004001101	500 mL in 1 BOTTLE, PUMP (83004-011-01)Marketed from May 30, 2024

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): Anti Fungal Foot and Body
Generic name (nonproprietary): sepia officinalis juice,melaleuca alternifolia
Active ingredients: Sepia officinalis juice — 12 [hp_X]/mLTea tree oil — .04 g/mL
Dosage form: Liquid
Route: Topical
Labeler: Rida LLCNDC labeler code 83004
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 30, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 83004-011_407ee691-b648-b0ec-e063-6294a90ac5efSPL ID 407ee691-b648-b0ec-e063-6294a90ac5efSPL set ID d3b12772-43e1-452d-9aa0-65cbd9745484UNII QDL83WN8C2, VIF565UC2G

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483004001101 followed by a unit qualifier and the quantity

Package 83004-0011-01. 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 Oct 6, 2025.

Indications (excerpt from the label)

Uses For the treatment of most ● jock itch (tinea cruris) ● ringworm (tinea corporis) ● athlete's foot (tinea pedis) ● tinea versicolor For relief of: ● itching ● scaling ● cracking ● burning ● irritation

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83004-011

What is NDC 83004-011?: 83004-011 is the product NDC for Anti Fungal Foot and Body, Sepia officinalis juice 12 [hp_X]/mL; Tea tree oil .04 g/mL liquid, listed with the FDA by Rida LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Anti Fungal Foot and Body (SEPIA OFFICINALIS JUICE,melaleuca alternifolia).
What is the active ingredient?: Sepia officinalis juice, Tea tree oil.
Who is the labeler?: Rida LLC, NDC labeler code 83004. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Anti Fungal Foot and Body?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.