NDC codes

FDA NDC Directory
Product NDC (as listed)58411-966Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58411-0966Add 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
58411-966-60584110966601 TUBE in 1 BOX (58411-966-60) / 50 mL in 1 TUBEMarketed from Sep 1, 2018

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

Generic name (nonproprietary)
octinoxate, titanium dioxide
Active ingredients
Octinoxate — 4.255 g/50mLTitanium dioxide — 3.0475 g/50mL
Dosage form
Cream
Route
Topical
Labeler
Shiseido Americas CorporationNDC labeler code 58411
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 040
Marketing start
Listing expires
Identifiers
Product ID 58411-966_4a2ca917-25ec-4dd4-e063-6294a90a7c48SPL ID 4a2ca917-25ec-4dd4-e063-6294a90a7c48SPL set ID 54f63dd8-e77f-42e4-a6d3-61ab7beecf50UNII 4Y5P7MUD51, 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

N458411096660 followed by a unit qualifier and the quantity

Package 58411-0966-60. 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)

Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58411-966

What is NDC 58411-966?
58411-966 is the product NDC for Shiseido Waso Color-Smart Day Moisturizer, Octinoxate 4.255 g/50mL; Titanium dioxide 3.0475 g/50mL cream, listed with the FDA by Shiseido Americas Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Shiseido Waso Color-Smart Day Moisturizer (Octinoxate, Titanium dioxide).
What is the active ingredient?
Octinoxate, Titanium dioxide.
Who is the labeler?
Shiseido Americas Corporation, NDC labeler code 58411. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Shiseido Waso Color-Smart Day Moisturizer?
1 other product NDC are listed under this name. See all Shiseido Waso Color-Smart Day Moisturizer NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Shiseido Waso Color-Smart Day Moisturizer NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Shiseido Waso Color-Smart Day Moisturizeroctinoxate, titanium dioxideOctinoxate 3.9553 g/50mL; Titanium dioxide 2.833 g/50mLCreamTopicalShiseido Americas Corporation58411-96458411-0964-60

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