What is NDC 85819-441?

85819-441 is the product NDC for Whitening Sunscreenanti Wrinkle, Water 52.49 g/1; Titanium dioxide 8 g/1 cream, listed with the FDA by Shantou Oushiya Biotechnology Co.,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

Shantou Oushiya Biotechnology Co.,Ltd, NDC labeler code 85819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Whitening Sunscreenanti Wrinkle?

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.

Whitening Sunscreenanti Wrinkle NDC 85819-441

NDC codes

FDA NDC Directory

Product NDC (as listed)85819-441Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85819-0441Add 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
85819-441-02	85819044102	5 APPLICATOR in 1 BOX (85819-441-02) / 1 CREAM in 1 APPLICATORMarketed from May 21, 2026

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): Whitening Sunscreenanti Wrinkle
Generic name (nonproprietary): whitening sunscreenanti wrinkle
Active ingredients: Water — 52.49 g/1Titanium dioxide — 8 g/1
Dosage form: Cream
Route: Topical
Labeler: Shantou Oushiya Biotechnology Co.,LtdNDC labeler code 85819
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 21, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 85819-441_524384e9-b3f9-4c13-e063-6394a90a8973SPL ID 524384e9-b3f9-4c13-e063-6394a90a8973SPL set ID 524384e9-b3f8-4c13-e063-6394a90a8973UNII 059QF0KO0R, 15FIX9V2JP

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

N485819044102 followed by a unit qualifier and the quantity

Package 85819-0441-02. 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 May 20, 2026.

Indications (excerpt from the label)

Before going out on a daily basis,take an appropriate amount of this product and apply it evenly to the face(avoiding sensitive areas around the eyes),neck,arms,and leg skin.Gently apply evenly.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85819-441

What is NDC 85819-441?: 85819-441 is the product NDC for Whitening Sunscreenanti Wrinkle, Water 52.49 g/1; Titanium dioxide 8 g/1 cream, listed with the FDA by Shantou Oushiya Biotechnology Co.,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Whitening Sunscreenanti Wrinkle.
What is the active ingredient?: Water, Titanium dioxide.
Who is the labeler?: Shantou Oushiya Biotechnology Co.,Ltd, NDC labeler code 85819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Whitening Sunscreenanti Wrinkle?: 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.