NDC codes

FDA NDC Directory
Product NDC (as listed)50814-063Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50814-0063Add 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
50814-063-015081400630150814006301473 mL in 1 BOTTLE (50814-063-01)Marketed from Aug 1, 2020
50814-063-025081400630250814006302946 mL in 1 BOTTLE (50814-063-02)Marketed from Aug 1, 2020

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)
alcohol
Active ingredients
Alcohol — .7 mL/mL
Dosage form
Gel
Route
Topical
Labeler
GFA Production (Xiamen) Co., Ltd.NDC labeler code 50814
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Identifiers
Product ID 50814-063_247f0f72-f854-6b93-e063-6394a90a84f7SPL ID 247f0f72-f854-6b93-e063-6394a90a84f7SPL set ID af8466d7-794a-cb95-e053-2a95a90a6ffcRxCUI 581662UNII 3K9958V90M

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

N450814006301 followed by a unit qualifier and the quantity

Package 50814-0063-01. 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)

Uses For hand washing to decrease bacteria on the skin that may cause disease. Recommended for repeated use.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50814-063

What is NDC 50814-063?
50814-063 is the product NDC for Genuine First Aid Hand Sanitizer Ethyl Alcohol, Alcohol .7 mL/mL gel, listed with the FDA by GFA Production (Xiamen) Co., Ltd.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Genuine First Aid Hand Sanitizer Ethyl Alcohol (Alcohol).
What is the active ingredient?
Alcohol.
Who is the labeler?
GFA Production (Xiamen) Co., Ltd., NDC labeler code 50814. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Genuine First Aid Hand Sanitizer Ethyl Alcohol?
1 other product NDC are listed under this name. See all Genuine First Aid Hand Sanitizer Ethyl Alcohol 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 Genuine First Aid Hand Sanitizer Ethyl Alcohol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Genuine First Aid Hand Sanitizer Ethyl AlcoholalcoholAlcohol .7 mL/mLGelTopicalGFA Production (Xiamen) Co., Ltd.50814-06050814-0060-0150814-0060-0250814-0060-03

Other NDCs under 505G(a)(3)

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

FDA NDC Directory listings under 505G(a)(3)
ProductStrengthForm · routeLabelerProduct NDC
Touchland Power Mist Spiced Pumpkin tini Scented Hydrating Hand sanitizeralcoholAlcohol 70 mL/100mLSprayTopicalChurch & Dwight Co., Inc.10237-117
DrugStore Antibacterial Hand Wipesbenzalkonium chlorideBenzalkonium chloride .13 g/100gClothTopicalLil' Drug Store Products, Inc.29485-6666
EcolabalcoholAlcohol 62 mL/100mLSolutionTopicalEcolab Inc.47593-472
Covex Antibacterial Bar Fresh Protectionbenzalkonium chlorideBenzalkonium chloride 1.3 mg/gSoapTopicalDALAN KIMYA ENDUSTRI ANONIM SIRKETI51209-020
Anti Bacterial Hand Gel Cookie Butter TrufflealcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-6759
Anti Bacterial Hand Gel Strawberry KiwialcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-7020
Hyvee LHSbwenzalkonium chlorideBenzalkonium chloride 130 mg/100mLLiquidTopicalApollo Health and Beauty Care63148-326
Benzalkonium chlorideBenzalkonium chloride 1.3 mg/mLLiquidTopicalPharmacy Value Alliance, LLC68016-866
Lavender ALOE HAND SANITIZERalcoholAlcohol .62 mL/mLGelTopicalK7 Design Group Inc.74177-025
hair treatmentminoxidilMinoxidil 1 mg/473mLCreamTopicalLABORATORIO MK SRL87022-009
SoftSoap Antibacterial with moisturizers Fresh Citrusbenzalkonium chlorideBenzalkonium chloride 1.33 mg/mLLiquidTopicalColgate-Palmolive Company35000-087
MediChoice PVP Prep Solutionpovidone-iodinePovidone-iodine 100 mg/mLSolutionTopicalO&M HALYARD, INC.39892-0841
Tartar control pluseucalyptol, menthol, methyl salicylate, thymolEucalyptol .92 mg/mL + 3 more ingredientsMouthwashOralUnited Natural Foods, Inc. dba UNFI41163-855
Covex Antibacterial Bar Active Protectionbenzalkonium chlorideBenzalkonium chloride 1.3 mg/gSoapTopicalDALAN KIMYA ENDUSTRI ANONIM SIRKETI51209-017
everyone hand sanitizer wipes ruby grapefruitethyl alcoholAlcohol 62 mL/100mLClothTopicalEO Products, LLC54748-703
Povidone-Iodine Prep Sterilepovidone-iodinePovidone-iodine 100 mg/gSpongeTopicalChangzhou Maokang Medical Products Co., Ltd59050-658
Anti Bacterial Hand Gel Bright Christmas MorningalcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-6758
Iced Lemon Pound Cake Pistachio Milk and HoneyalcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-7018
Hy-Vee LHSbenzalkonium chlorideBenzalkonium chloride 130 mg/100mLLiquidTopicalApollo Health and Beauty Care63148-316
Smart Care 2 HAND SANITIZERS 1.35 FL OZ (PUMPKIN SPICE, FRESH RAIN)ethyl alcohol—KitAshtel Studios, Inc.70108-372

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