What is NDC 84417-002?

84417-002 is the product NDC for Fitish SPF 50 Face, Octinoxate 7.5 g/100g + 2 more ingredients stick, listed with the FDA by Fitish Holdings, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Octinoxate, Octocrylene, Octisalate.

Fitish Holdings, LLC, NDC labeler code 84417. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fitish SPF 50 Face?

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.

Fitish SPF 50 Face NDC 84417-002 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)84417-002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84417-0002Add 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
84417-002-01	84417000201	50 g in 1 BOTTLE (84417-002-01)Marketed from Jun 26, 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): Fitish SPF 50 Face
Generic name (nonproprietary): fitish spf 50 face
Active ingredients: Octinoxate — 7.5 g/100gOctocrylene — 8 g/100gOctisalate — 5 g/100g
Dosage form: Stick
Route: Cutaneous
Labeler: Fitish Holdings, LLCNDC labeler code 84417
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 26, 2024
Listing expires: Dec 31, 2027
Identifiers: Product ID 84417-002_569ce846-37d3-9a7d-e063-6394a90a6309SPL ID 569ce846-37d3-9a7d-e063-6394a90a6309SPL set ID 1c44a572-59e6-c3c5-e063-6394a90a0e24UNII 4Y5P7MUD51, 5A68WGF6WM, 4X49Y0596W

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N484417000201 followed by a unit qualifier and the quantity

Package 84417-0002-01. 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 Jul 14, 2026.

Indications (excerpt from the label)

Use USES Helps prevent sunburn

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 84417-002

What is NDC 84417-002?: 84417-002 is the product NDC for Fitish SPF 50 Face, Octinoxate 7.5 g/100g + 2 more ingredients stick, listed with the FDA by Fitish Holdings, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fitish SPF 50 Face.
What is the active ingredient?: Octinoxate, Octocrylene, Octisalate.
Who is the labeler?: Fitish Holdings, LLC, NDC labeler code 84417. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fitish SPF 50 Face?: 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.