NDC codes

FDA NDC Directory
Product NDC (as listed)71217-0060Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71217-0060Add 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 NDC11-digit (billing)PackageCopy
71217-0060-17121700600150 mL in 1 TUBE (71217-0060-1)Marketed from Jan 15, 2023
71217-0060-27121700600215 mL in 1 TUBE (71217-0060-2)Marketed from Jan 15, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Protecting base suncream
Generic name (nonproprietary)
citronellol, geraniol, linalool
Active ingredients
Niacinamide — 2 g/100mLAdenosine — .04 g/100mL
Dosage form
Cream
Route
Topical
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Other FDA classes
Adenosine Receptor Agonists (Mechanism)
Identifiers
Product ID 71217-0060_f3856fda-71d3-2703-e053-2995a90a17a8SPL ID f3856fda-71d3-2703-e053-2995a90a17a8SPL set ID f3856094-a55a-6982-e053-2a95a90accb2UNII 25X51I8RD4, K72T3FS567
Pharmacologic class
Adenosine Receptor Agonist

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

N471217006001 followed by a unit qualifier and the quantity

Package 71217-0060-01. 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 .

Indications (excerpt from the label)

apply generously to ensure coverage on your face and neck approximately 30 minutes prior to outdoor activity recommended to re-apply every two hours, if exposed to the sun

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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