Over-the-counter drug · OTC MONOGRAPH DRUG

Menthol (Maximum strength medicated foot powder) NDC 63941-558

Menthol 2.8 g/283g · Powder · Topical · VALU MERCHANDISERS, CO

NDC codes

FDA NDC Directory
Product NDC (as listed)63941-558Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63941-0558Add 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
63941-558-106394105581063941055810283 g in 1 BOTTLE, PLASTIC (63941-558-10)Marketed from Jul 15, 2019

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)
Menthol
Generic name (nonproprietary)
maximum strength medicated foot powder
Active ingredients
Menthol — 2.8 g/283g
Dosage form
Powder
Route
Topical
Labeler
VALU MERCHANDISERS, CONDC labeler code 63941
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 017
Marketing start
Marketing end
Identifiers
Product ID 63941-558_445c7a07-4f2a-f717-e063-6394a90ac462SPL ID 445c7a07-4f2a-f717-e063-6394a90ac462SPL set ID 89a5c4bb-442f-d3f0-e053-2a95a90a51bdRxCUI 259579UNII L7T10EIP3A

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

N463941055810 followed by a unit qualifier and the quantity

Package 63941-0558-10. 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)

​Use for the temporary relief of pain and itching associated with minor skin irritations

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63941-558

What is NDC 63941-558?
63941-558 is the product NDC for Menthol (maximum strength medicated foot powder), Menthol 2.8 g/283g powder, listed with the FDA by VALU MERCHANDISERS, CO. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Menthol (Maximum Strength Medicated Foot Powder).
What is the active ingredient?
Menthol.
Who is the labeler?
VALU MERCHANDISERS, CO, NDC labeler code 63941. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Menthol?
10 other product NDCs are listed under this name. See all Menthol 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 Menthol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MentholMenthol, Unspecified form 4 g/100mLGelTopicalCHEMCO CORPORATIOM49283-57749283-0577-03
MentholMenthol, Unspecified form 4 g/100mLGelTopicalSUNSET PAIN RELIEF72937-63272937-0632-03
MentholMenthol .01 g/100mLPasteTopicalFlexiGo Inc85524-251085524-2510-0685524-2510-09
Mentholmaximum strength medicated foot powder talc freeMenthol 10 mg/gPowderTopicalTarget Corporation82442-21182442-0211-01
Mentholmaximum strength medicated foot powder talc freeMenthol 10 mg/gPowderTopicalFSA Store Inc.81522-06981522-0069-01
Mentholcough suppressantMenthol, Unspecified form .86 g/gLozengeOralMcKesson68599-046568599-0465-09
Mentholcough suppressantMenthol, Unspecified form .7 g/gLozengeOralMcKesson68599-046468599-0464-09
MentholMenthol, Unspecified form 4 g/100mLGelTopicalSUNSET PAIN RELIEF ROLL-ON 3OZ72937-00472937-0004-03
Mentholmaximum strength medicated foot powder talc freeMenthol 2.8 g/283gPowderTopicalTopco Associates LLC36800-25236800-0252-10
Mentholamish origins medicatedMenthol 8 g/100gCreamTopicalAmish Origins LLC62212-25262212-0252-0162212-0252-0262212-0252-03+1 more

Other NDCs under M 017

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

FDA NDC Directory listings under M 017
ProductStrengthForm · routeLabelerProduct NDC
Extra Strength Itch Reliefdiphenhydramine hcl and zinc acetateDiphenhydramine hydrochloride 20 mg/g; Zinc acetate 1 mg/gSprayTopicalMeijer Distribution Inc79481-0598
3X Medicated Toothache and Gum GelbenzocaineBenzocaine 20 g/100g + 2 more ingredientsGelOralRite Aid11822-0613
Meijer Pain Relieving Balm Analgesictrolamine salicylateTrolamine salicylate 10 mg/gCreamTopicalMeijer Distribution, Inc41250-356
Ralli Rapid Pain Relief Roll onmentholMenthol 100 mg/mLGelTopicalTroy Manufacturing, Inc.63936-9527
CVS Health Pain Relievingcamphor (synthetic), menthol (unspecified form), methyl salicylateCamphor (Synthetic) 28 mg/1 + 2 more ingredientsPatchTransdermalNatural Essentials, Inc.66902-280
Pbz Otctripelennamine hcl 1%Tripelennamine 1 g/100gCreamTopicalKingsway Pharmaceuticals dba NFI, LLC69993-151
HydrocortisoneHydrocortisone 1 g/100gCreamTopicalHenry Schein0404-0166
American Safety and First Aidhydrocortisone acetateHydrocortisone acetate 10 mg/gCreamTopicalOrazen Inc71927-015
MyDerm Bite ReliefbenzocaineBenzocaine 5 g/100gOintmentTopicalInspec Solutions LLC.72667-019
Thera Plus Maximum Strength HydrocortisonehydrocortisoneHydrocortisone 10 mg/gCreamTopicalFourstar Group USA, Inc80684-197
Lidocaine 4%Lidocaine 400 mg/10gPatchTransdermalMarcella Health85096-201
Tough Love Pain Relievinglidocaine hclLidocaine 4 g/100gCreamTopicalAllure Labs62742-4222
Stopain Extra Strength GelmentholMenthol 80 mg/mLGelTopicalTroy Manufacturing, Inc.63936-9506
Fast Freeze Lidocaine Roll-Onlidocaine hydrochloride, benzyl alcoholLidocaine hydrochloride 40 mg/mL; Benzyl alcohol 10 mg/mLLiquidTopicalNatural Essentials, Inc.66902-235
Walgreens pain relievinglidocaine 4%Lidocaine 4 g/100gAerosol, SprayTopicalWalgreens0363-3038
Bikini Zone Medicated CremelidocaineLidocaine 2 g/100gCreamTopicalKingsway Pharmaceuticals dba NFI, LLC69993-043
American Safety First Aidlidocaine hclLidocaine hydrochloride 20 mg/mLSprayTopicalOrazen Inc71927-012
ACOLYE Lidocaine Cream Topical Analgesia Creamlidocaine,mentholLidocaine 4 g/100g; Menthol 1 g/100gCreamTopicalGuangdong Aimu Biological Technology Co., Ltd83566-617
Healmusz Eczemahydrocortisone 1% eczemaHydrocortisone 1 g/100gCreamTopicalJiangxi Yudexi Pharmaceutical Co., LTD85248-203
ELAIMEI Numbing Creamlidocaine 4%Lidocaine 4 g/100mLCreamTopicalShenzhen Shandian Jingling Technology Co., Ltd.83804-005

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