What is NDC 87735-003?

87735-003 is the product NDC for SULISRx Sunburn Relief Kit (sunburn relief kit) kit, listed with the FDA by Sephoris Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

SULISRx Sunburn Relief Kit (Sunburn Relief Kit).

Sephoris Pharmaceuticals, LLC, NDC labeler code 87735. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for SULISRx Sunburn Relief Kit?

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.

SULISRx Sunburn Relief Kit NDC 87735-003

NDC codes

FDA NDC Directory

Product NDC (as listed)87735-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87735-0003Add 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
87735-003-01	87735000301	1 KIT in 1 KIT (87735-003-01) * 59 mL in 1 BOTTLE, SPRAY (87735-001-01) * 1 TABLET, FILM COATED in 1 BOTTLE (87735-002-01)Marketed from Sep 3, 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): SULISRx Sunburn Relief Kit
Generic name (nonproprietary): sunburn relief kit
Dosage form: Kit
Labeler: Sephoris Pharmaceuticals, LLCNDC labeler code 87735
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Sep 3, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 87735-003_5bd70084-eba8-42c4-e063-6294a90afb34SPL ID 5bd70084-eba8-42c4-e063-6294a90afb34

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

N487735000301 followed by a unit qualifier and the quantity

Package 87735-0003-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 87735-003

What is NDC 87735-003?: 87735-003 is the product NDC for SULISRx Sunburn Relief Kit (sunburn relief kit) kit, listed with the FDA by Sephoris Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: SULISRx Sunburn Relief Kit (Sunburn Relief Kit).
Who is the labeler?: Sephoris Pharmaceuticals, LLC, NDC labeler code 87735. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for SULISRx Sunburn Relief Kit?: 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.

SULISRx Sunburn Relief Kit (Sunburn relief kit) NDC 87735-003