What is NDC 85897-374?

85897-374 is the product NDC for Body / Face Sunscreen Sun, Homosalate 7.5 g/1; Octinoxate 7.5 g/1 cream, augmented, listed with the FDA by Guanghzou AiXin Biotech Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

Guanghzou AiXin Biotech Co., Ltd, NDC labeler code 85897. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Body / Face Sunscreen 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.

Body / Face Sunscreen Sun NDC 85897-374

NDC codes

FDA NDC Directory

Product NDC (as listed)85897-374Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85897-0374Add 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
85897-374-01	85897037401	5 BAG in 1 BOX (85897-374-01) / 1 CREAM, AUGMENTED in 1 BAGMarketed from Jul 8, 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): Body / Face Sunscreen Sun
Generic name (nonproprietary): body / face sunscreen sun
Active ingredients: Homosalate — 7.5 g/1Octinoxate — 7.5 g/1
Dosage form: Cream, Augmented
Route: Cutaneous
Labeler: Guanghzou AiXin Biotech Co., LtdNDC labeler code 85897
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 3, 2025
Listing expires: Dec 31, 2027
Identifiers: Product ID 85897-374_4d372a4d-ba8f-b8e4-e063-6294a90ae9d8SPL ID 4d372a4d-ba8f-b8e4-e063-6294a90ae9d8SPL set ID 39035b99-e560-e6b6-e063-6294a90a19c6UNII V06SV4M95S, 4Y5P7MUD51

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

N485897037401 followed by a unit qualifier and the quantity

Package 85897-0374-01. 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 Mar 17, 2026.

Indications (excerpt from the label)

Sunscreen

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85897-374

What is NDC 85897-374?: 85897-374 is the product NDC for Body / Face Sunscreen Sun, Homosalate 7.5 g/1; Octinoxate 7.5 g/1 cream, augmented, listed with the FDA by Guanghzou AiXin Biotech Co., Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Body / Face Sunscreen Sun.
What is the active ingredient?: Homosalate, Octinoxate.
Who is the labeler?: Guanghzou AiXin Biotech Co., Ltd, NDC labeler code 85897. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Body / Face Sunscreen 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.