NDC codes

FDA NDC Directory
Product NDC (as listed)72839-083Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72839-0083Add 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
72839-083-087283900830872839008308227 g in 1 BOTTLE, PLASTIC (72839-083-08)Marketed from Nov 25, 2021
72839-083-187283900831872839008318227 g in 1 BOTTLE, PLASTIC (72839-083-18)Marketed from Nov 25, 2021
72839-083-287283900832872839008328227 g in 1 BOTTLE, PLASTIC (72839-083-28)Marketed from Nov 25, 2021
72839-083-387283900833872839008338227 g in 1 BOTTLE, PLASTIC (72839-083-38)Marketed from Nov 25, 2021

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)
Aruba Sun SPF 50 Sunscreen
Generic name (nonproprietary)
avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10%
Active ingredients
Octisalate — 5 g/100gAvobenzone — 3 g/100gOctocrylene — 10 g/100gHomosalate — 15 g/100g
Dosage form
Lotion
Route
Topical
Labeler
Derma Care Research Labs, LLCNDC labeler code 72839
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 020
Marketing start
Listing expires
Identifiers
Product ID 72839-083_29a4c95d-6cdf-955f-e063-6294a90a1846SPL ID 29a4c95d-6cdf-955f-e063-6294a90a1846SPL set ID d8b28ce6-e938-c6e3-e053-2a95a90acc29UNII 4X49Y0596W, G63QQF2NOX, 5A68WGF6WM, V06SV4M95SUPC 0665871078437, 0665871149694, 0093423880182, 0665871022140

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

N472839008308 followed by a unit qualifier and the quantity

Package 72839-0083-08. 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)

Directions Apply liberally 15 minutes before sun exposure. Reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours Sun protection measures: spending time n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including: limit time in the sun, especially from 10 am to 2 pm wear long-sleeved shirts, pants, hats, and sunglasses. Children under 6 months: ask a doctor.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72839-083

What is NDC 72839-083?
72839-083 is the product NDC for Aruba Sun SPF 50 Sunscreen, Octisalate 5 g/100g + 3 more ingredients lotion, listed with the FDA by Derma Care Research Labs, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Aruba Sun SPF 50 Sunscreen (Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%).
What is the active ingredient?
Octisalate, Avobenzone, Octocrylene, Homosalate.
Who is the labeler?
Derma Care Research Labs, LLC, NDC labeler code 72839. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aruba Sun SPF 50 Sunscreen?
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.

Other NDCs under M 020

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under M 020
ProductStrengthForm · routeLabelerProduct NDC
bareMinerals Original Foundation Broad Spectrum SPF 15 Light 08titanium dioxide and zinc oxideTitanium dioxide 1440 mg/8g; Zinc oxide 1760 mg/8gPowderTopicalOrveon Global US LLC98132-010
BelleJoss BROAD SPECTRUM SPF 50broad spectrum spf 50Ethylhexyl methoxycinnamate 7.4925 mg/100mgCreamTopicalGuangzhou Liyan Cosmetics Technology Co., Ltd.87770-002
Mineral Based Foam Sunscreen Non-Tintedtitanium dioxide, zinc oxideTitanium dioxide 30 mg/g; Zinc oxide 100 mg/gAerosol, FoamTopicalKATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION81679-211
COOLA Classic Body SPF 50 Guava Mangoavobenzone, homosalate, octisalate, octocryleneAvobenzone 2.9 g/100mL + 3 more ingredientsSprayTopicalCOOLA, LLC79753-059
Golden Rose Glow Kiss Tinted Lip Balm Vanilla Latteavobenzone, octinoxateAvobenzone 2.7 g/100g; Octinoxate 6 g/100gLipstickTopicalERKUL KOZMETIK SANAYI VE TICARET ANONIM SIRKETI82715-109
Restore Plus Defense Acne Safe Facial Mineral Sunscreen Lightly Tintedzinc oxideZinc oxide 160 mg/gCreamTopicalNY BEAUTY PALACE LLC85404-208
Tinted Mineral Sunscreentitanium dioxide, zinc oxideTitanium dioxide 80 mg/g; Zinc oxide 38 mg/gCreamTopicalThe Essential Brazilian Spa LLC85492-203
Tinted Sunscreentitanium dioxide, zinc oxideTitanium dioxide 80 mg/g; Zinc oxide 38 mg/gCreamTopicalScottsdale Skin Boutique and Dermatology Pllc85331-203
First Aid Beauty FAB Ultra Light Mineral Sunscreen Broad Spectrum SPF 30zinc oxideZinc oxide 22 g/100mLLiquidTopicalThe Procter & Gamble Manufacturing Company84126-214
the beach people SPF 15zinc oxideZinc oxide 12 g/100mLLotionTopicalThe Beach People United LLC84530-100
Tinted Sunscreen Broad SPF30Zinc oxide 7.5 g/100g; Titanium dioxide 3.2 g/100gCreamTopicalDOSCHER FAMILY HEALTH NP P.C.84608-0651
Flawless Future SPF 30octinoxate, octisalate, oxybenzone, avaobenzoneOctinoxate 7.14 mg/g + 3 more ingredientsEmulsionTopicalREVLON10967-683
Lbel Forever Matte Base Control Brillo Y Larga Duracion 48H Fps 15 Control And Longwear Foundation 48H SPF 15 Latte 180-Foctinoxate, zinc oxideOctinoxate 50 mg/g; Zinc oxide 49 mg/gEmulsionTopicalBEL STAR S.A.14141-342
Pro-Tect Sports Sunscreenmeradimate, octinoxate, octisalate, oxybenzoneOctinoxate 75 mg/g + 3 more ingredientsLotionCutaneousBio-Medical & Pharmaceutical Manufacturing Corporation37945-862
ZO Skin Health Sunscreen Plus Primer Broad-Spectrum SPF 30titanium dioxide and zinc oxideTitanium dioxide 10 mg/mL; Zinc oxide 200 mg/mLCreamTopicalZO Skin Health, Inc.42851-060
Artistry Exact Fit Longwearing Foundation Shade Golden L4N1titanium dioxideTitanium dioxide 40.25 mg/mLCreamTopicalAmway Corp50390-205
Derma B Everyday Fit Sunscreen SPF 50avobezone, homosalate, octisalate, octocryleneAvobenzone 30 mg/mL + 3 more ingredientsLotionTopicalNeoPharm Co., Ltd.51141-0701
Cell Fusion C Laser UV Defense Sunscreen Broad Spectrum SPF 50homosalate, octisalate, octocrylene, zinc oxideHomosalate 6 g/50mL + 3 more ingredientsCreamTopicalCMS LAB Inc.52554-9062
SPF 30 Sunscreenavobenzone, homosalate, octisalate, octocryleneAvobenzone 30 mg/g + 3 more ingredientsAerosol, SprayTopicalDEMOULAS SUPER MARKETS, INC53942-002
Amazonian Clay BB Tinted Moisturizer Broad Spectrum SPF 20 Sunscreen Ivorytitanium dioxide and zinc oxideTitanium dioxide 50 mg/mL; Zinc oxide 50 mg/mLCreamTopicalPML NYC, LLC59735-900

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