NDC codes

FDA NDC Directory
Product NDC (as listed)82944-104Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82944-0104Add 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
82944-104-10829440104108294401041010 POUCH in 1 BOX (82944-104-10) / 1 PATCH in 1 POUCHMarketed from Oct 1, 2023

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)
Lidosync
Generic name (nonproprietary)
lidocaine 4%, menthol 1%
Active ingredients
Lidocaine — 4 g/1Menthol — 1 g/1
Dosage form
Patch
Route
Topical
Labeler
Ion Pharma, LLCNDC labeler code 82944
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Other FDA classes
Amides (Chemical structure)Local Anesthesia (Physiologic effect)
Identifiers
Product ID 82944-104_556e3beb-c7f7-b0fc-e063-6294a90afe5bSPL ID 556e3beb-c7f7-b0fc-e063-6294a90afe5bSPL set ID 11116755-885e-4cce-bc4c-d87a2baadda4RxCUI 1249758UNII 98PI200987, L7T10EIP3AUPC 0382944104106
Pharmacologic class
Amide Local Anesthetic; Antiarrhythmic

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

N482944010410 followed by a unit qualifier and the quantity

Package 82944-0104-10. 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)

Drug Facts Active ingredients: Lidocaine 4% Menthol 1% Purpose Topical anesthetic - Topical analgesic INDICATIONS & USAGE Uses: For temporary relief of pain. Warnings For external use only DO NOT USE Do not use: More than one patch on your body at a time - On wounds or damaged skin - For more than one week without consulting a doctor - If you are allergic to any ingredients of this product. WHEN USING When using this product: Use only as directed - Avoid contact with the eyes, mucous membranes or rashes - Do not bandage tightly STOP USE Stop use and consult a doctor if: Localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering - Conditions wors…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82944-104

What is NDC 82944-104?
82944-104 is the product NDC for Lidosync, Lidocaine 4 g/1; Menthol 1 g/1 patch, listed with the FDA by Ion Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lidosync (Lidocaine 4%, Menthol 1%).
What is the active ingredient?
Lidocaine, Menthol.
Who is the labeler?
Ion Pharma, LLC, NDC labeler code 82944. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lidosync?
1 other product NDC are listed under this name. See all Lidosync 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 Lidosync NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LidoSynclidocaine, mentholLidocaine hydrochloride anhydrous 3.1 g/76.5g; Levomenthol .8 g/76.5gCreamTopicaliON Pharma, LLC82944-20082944-0200-01

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)
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Smart Care TEA and TIMBER HAND SANITIZERethyl alcoholAlcohol 70 mL/100mLSprayTopicalAshtel Studios, Inc.70108-199
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VQ Hydrating Hand Sanitizer Frosted Candy ApplealcoholAlcohol 67.5 mL/100mLLiquidTopicalTychea Co.85980-024
BCBG GENERATION HAND SANITIZER DUO - WILD Cherry AND Mango Cherry SCENTethyl alcohol—KitDiamond Life Cosmetics Trading FZCO87247-933
Anti Bacterial Hand Gel GinghamalcoholAlcohol 71 mL/100mLGelTopicalBath & Body Works, Inc.62670-6641
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Povidone-Iodine Prep Winged Sterile Largepovidone-iodinePovidone-iodine 100 mg/gSpongeTopicalCardinal Health 200, Inc63517-759
Smart-San Hand Sanitizer FoamalcoholAlcohol 74 mL/100mLLiquidTopicalBest Sanitizers, Inc.59900-352
BZK Antiseptic Towelette Sterilebenzalkonium chlorideBenzalkonium chloride 1.3 mg/gClothTopicalJianerkang Medical Co., Ltd34645-0018
Lavender Hand Sanitizing WipesethanolAlcohol 65 mL/100mLClothTopicalWhole Foods Market, Inc.42681-6810
Pacific Blue ultra Antimicrobial Foam Fragrance Freebenzalkonium chlorideBenzalkonium chloride .13 g/100mLSolutionTopicalGeorgia-Pacific Consumer Products54622-316
Zylast Antiseptic Sethyl alcoholAlcohol 760 mL/1000mLLiquidTopicalInnovative BioDefense57362-466
WhiskCare 375alcoholAlcohol 600 mL/LGelTopicalWhisk Products, Inc.65585-375
GuruNanda Healthy Gumscetylpyridinium chlorideCetylpyridinium chloride 1 mg/mLMouthwashOralGURUNANDA, LLC70708-926
Smart Care SWEET AND STILL HAND SANITIZERethyl alcoholAlcohol 70 mL/100mLSprayTopicalAshtel Studios, Inc.70108-192
B-Pure Moisturizing Hand Sanitizer Midnight Freesia ScentedalcoholAlcohol 70 mL/100mLLiquidTopicalFourstar Group USA, Inc.80684-214
RootStim Minoxidil Hair Regrowth TreatmentminoxidilMinoxidil 5 g/100mLLiquidTopicalYITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD83364-025

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