NDC codes

FDA NDC Directory
Product NDC (as listed)46581-670Labeler and product segments. Claims need a package NDC.
Product NDC at billing width46581-0670Add 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
46581-670-0146581067001465810670011 PATCH in 1 POUCH (46581-670-01)Marketed from Jul 6, 2011
46581-670-0346581067003465810670033 PATCH in 1 POUCH (46581-670-03)Marketed from Sep 26, 2008
46581-670-0546581067005465810670051 POUCH in 1 BOX (46581-670-05) / 5 PATCH in 1 POUCHMarketed from May 22, 2008
46581-670-0646581067006465810670062 POUCH in 1 BOX (46581-670-06) / 3 PATCH in 1 POUCHMarketed from Dec 31, 2013
46581-670-1546581067015465810670153 POUCH in 1 BOX (46581-670-15) / 5 PATCH in 1 POUCHMarketed from Jun 26, 2008
46581-670-2046581067020465810670204 POUCH in 1 BOX (46581-670-20) / 5 PATCH in 1 POUCHMarketed from Feb 1, 2020
46581-670-9946581067099465810670991 PATCH in 1 POUCH (46581-670-99)Marketed from Jul 6, 2011

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)
Salonpas Pain Relief
Generic name (nonproprietary)
menthol, methyl salicylate
Active ingredients
Menthol — 31.5 mg/1Methyl salicylate — 105 mg/1
Dosage form
Patch
Route
Percutaneous, Topical, Transdermal
Labeler
Hisamitsu Pharmaceutical Co., Inc.NDC labeler code 46581
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 022029
Marketing start
Listing expires
Identifiers
Product ID 46581-670_b15d7bd2-d065-4a54-af88-27518cc59143SPL ID b15d7bd2-d065-4a54-af88-27518cc59143SPL set ID 724bc4d3-0bc1-4275-a23b-4bbc62fbc0d2RxCUI 853146UNII L7T10EIP3A, LAV5U5022Y

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

N446581067001 followed by a unit qualifier and the quantity

Package 46581-0670-01. 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 Temporarily relieves mild to moderate aches and pains of muscles and joints associated with: strains sprains simple backache arthritis bruises

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 46581-670

What is NDC 46581-670?
46581-670 is the product NDC for Salonpas Pain Relief, Menthol 31.5 mg/1; Methyl salicylate 105 mg/1 patch, listed with the FDA by Hisamitsu Pharmaceutical Co., Inc.. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Salonpas Pain Relief (Menthol, Methyl Salicylate).
What is the active ingredient?
Menthol, Methyl salicylate.
Who is the labeler?
Hisamitsu Pharmaceutical Co., Inc., NDC labeler code 46581. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Salonpas Pain Relief?
1 other product NDC are listed under this name. See all Salonpas Pain Relief 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 Salonpas Pain Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Salonpas Pain Reliefmenthol, methyl salicylateMenthol 63 mg/1; Methyl salicylate 210 mg/1PatchPercutaneous, Topical, TransdermalHisamitsu Pharmaceutical Co., Inc.46581-67546581-0675-0146581-0675-0946581-0675-99

Other NDCs under NDA 022029

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

FDA NDC Directory listings under NDA 022029
ProductStrengthForm · routeLabelerProduct NDC
NumbingmentholMenthol 3 g/100mL; Methyl salicylate 10 g/100mLCreamTopicalFlexiGo Inc85524-2605
Salonpas Arthritis Painmenthol, methyl salicylateMenthol 31.5 mg/1; Methyl salicylate 105 mg/1PatchPercutaneous, Topical, TransdermalHisamitsu Pharmaceutical Co., Inc.46581-680
Salonpas Arthritis Painmenthol, methyl salicylateMenthol 63 mg/1; Methyl salicylate 210 mg/1PatchPercutaneous, Topical, TransdermalHisamitsu Pharmaceutical Co., Inc.46581-685
Salonpas Pain Reliefmenthol, methyl salicylateMenthol 63 mg/1; Methyl salicylate 210 mg/1PatchPercutaneous, Topical, TransdermalHisamitsu Pharmaceutical Co., Inc.46581-675

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