What is NDC 85819-771?

85819-771 is the product NDC for Sensitive Pocket Sun, Talc 15 mg/1; Cyclopentasiloxane 26.5 mg/1 stick, 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 Sensitive Pocket Sun?

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.

Sensitive Pocket Sun NDC 85819-771 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85819-771Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85819-0771Add 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
85819-771-43	85819077143	5 BOTTLE, UNIT-DOSE in 1 BOX (85819-771-43) / 1 STICK in 1 BOTTLE, UNIT-DOSEMarketed from Jul 15, 2025

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): Sensitive Pocket Sun
Generic name (nonproprietary): sensitive pocket sun
Active ingredients: Talc — 15 mg/1Cyclopentasiloxane — 26.5 mg/1
Dosage form: Stick
Route: Percutaneous
Labeler: Shantou Oushiya Biotechnology Co., LtdNDC labeler code 85819
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 15, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 85819-771_37938cce-264a-b486-e063-6394a90a17b4SPL ID 37938cce-264a-b486-e063-6394a90a17b4SPL set ID 36ac412f-e31f-6906-e063-6394a90a4a3dUNII 7SEV7J4R1U, 0THT5PCI0RUPC 6974452889008

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

N485819077143 followed by a unit qualifier and the quantity

Package 85819-0771-43. 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 Jun 14, 2025.

Indications (excerpt from the label)

Rotate about 3mm and apply evenly to areas that are easily exposed to ultraviolet rays.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85819-771

What is NDC 85819-771?: 85819-771 is the product NDC for Sensitive Pocket Sun, Talc 15 mg/1; Cyclopentasiloxane 26.5 mg/1 stick, 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?: Sensitive Pocket Sun.
What is the active ingredient?: Talc, Cyclopentasiloxane.
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 Sensitive Pocket Sun?: 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.