What is NDC 87243-123?

87243-123 is the product NDC for Sunscreen, Octinoxate 1 g/1 cream, listed with the FDA by MAIDORA CO.,LTD. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sunscreen (Japanese Sunscreen SPF 50 Super Water Gel Sunscreen 4.22floz(125g) Refill).

MAIDORA CO.,LTD, NDC labeler code 87243. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sunscreen?

24 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sunscreen NDC 87243-123 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)87243-123Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87243-0123Add 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
87243-123-35	87243012335	5 CANISTER in 1 BOX (87243-123-35) / 1 CREAM in 1 CANISTERMarketed from Nov 21, 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): Sunscreen
Generic name (nonproprietary): japanese sunscreen spf 50 super water gel sunscreen 4.22floz(125g) refill
Active ingredients: Octinoxate — 1 g/1
Dosage form: Cream
Route: Cutaneous
Labeler: MAIDORA CO.,LTDNDC labeler code 87243
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 21, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 87243-123_44136f78-878a-8185-e063-6394a90ad848SPL ID 44136f78-878a-8185-e063-6394a90ad848SPL set ID 44136f78-8789-8185-e063-6394a90ad848UNII 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

N487243012335 followed by a unit qualifier and the quantity

Package 87243-0123-35. 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 Nov 20, 2025.

Indications (excerpt from the label)

helps prevent sunburn apply liberally 15 minutes before sun exposure after 80 minutes of swimming or sweating immediately after towel drying

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87243-123

What is NDC 87243-123?: 87243-123 is the product NDC for Sunscreen, Octinoxate 1 g/1 cream, listed with the FDA by MAIDORA CO.,LTD. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sunscreen (Japanese Sunscreen SPF 50 Super Water Gel Sunscreen 4.22floz(125g) Refill).
What is the active ingredient?: Octinoxate.
Who is the labeler?: MAIDORA CO.,LTD, NDC labeler code 87243. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sunscreen?: 24 other product NDCs are listed under this name. See all Sunscreen 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 Sunscreen NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	Charleston Dermatology, P.C.	87901-3019	87901-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	Concierge Choice LLC	87955-3019	87955-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	1226 W AESTHETICS	82031-3019	82031-3019-01
Sunscreenbroad spectrum spf 30	Octocrylene 5 g/100g + 2 more ingredients	SprayTopical	SKNVCARE, LLC	82704-3019	82704-3019-01
sunscreentitanium dioxide	Titanium dioxide 2.85 g/100mL; Ethylhexyl salicylate 3 g/100mL	LotionCutaneous	Guangdong Zhoubang Biotechnology Co., Ltd	87357-001	87357-0001-01
sunscreentitanium dioxide(nano)	Titanium dioxide 4 g/100g; Ethylhexyl methoxycinnamate 7.5 g/100g	LotionTopical	Mingyu (guangdong) Cosmetics Technology Co., Ltd	87091-001	87091-0001-01
Sunscreen	Avobenzone 30 mg/mL + 2 more ingredients	LotionTopical	Old East Main Co.	75712-950	75712-0950-30
Sunscreentitanium dioxide 6.8%	Titanium dioxide .068 g/mL	LiquidTopical	Baxter of California, LLC	84203-001	84203-0001-01
Sunscreenavobenzone, homosalate, octisalate	Avobenzone 30 mg/g + 2 more ingredients	SprayTopical	Retail Business Services, LLC	72476-949	72476-0949-14
Sunscreen	Avobenzone 30 mg/mL + 2 more ingredients	LotionTopical	Retail Business Services, LLC	72476-951	72476-0951-30

All 25 Sunscreen NDCs