Mentholatum Heel Revival Cream

Manufacturer
The Mentholatum Company
Effective date
2024-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:37:44

Label at a glance#

ProductMentholatum Heel Revival Cream
Active ingredientTOLNAFTATE
Label structure9 sections

Indications and uses

proven clinically effective in the treatment of most cracked heel athlete’s foot relieves cracking, irritation and discomfort prevents the recurrence of most cracked heel athlete's foot with daily use Clears up most athlete’s foot infection and with daily use helps keep it from coming back

Dosage and administration

clean the affected area and dry thoroughly apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor supervise children in the use of this product for athlete’s foot: pay special attention to the areas between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily for athlete's foot, use daily for 4 weeks. If condition per...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Tolnaftate - Antifungal

Uses

INDICATIONS & USAGE SECTION

  • proven clinically effective in the treatment of most cracked heel athlete’s foot
  • relieves cracking, irritation and discomfort
  • prevents the recurrence of most cracked heel athlete's foot with daily use
  • Clears up most athlete’s foot infection and with daily use helps keep it from coming back

Warnings

WARNINGS SECTION

For external use only

Do not use

WARNINGS SECTION

on children under 2 years of age unless directed by a doctor.

When using this product,

WARNINGS SECTION

avoid contact with the eyes.

Stop use and ask a doctor if

WARNINGS SECTION

  • irritation occurs
  • there is no improvement within 4 weeks

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area and dry thoroughly
  • apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor
  • supervise children in the use of this product
  • for athlete’s foot: pay special attention to the areas between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily
  • for athlete's foot, use daily for 4 weeks. If condition persists longer, consult a doctor
  • this product is not effective on the scalp or nails

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, caprylic/capric triglyceride, urea, cetyl alcohol, glycerin, glycine, hexadecane, tridecyl stearate, ethoxydiglycol, ceteth-23, polyacrylate crosspolymer-6, diethyl sebacate, dimethicone, hydroxyethylcellulose, lactic acid, phenoxyethanol, propylene glycol caprylate, simmondsia chinensis (jojoba) seed oil, sodium dilauramidoglutamide lysine, sorbitan stearate, squalane, zinc oxide

Questions?

OTC - QUESTIONS SECTION

1-877-636-2677 MON-FRI 9AM-5PM (EST)

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Central right away

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFrontPrinicipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
103951tolnaftate 1 % Topical CreamPSN1
103951tolnaftate 10 MG/ML Topical CreamSCD1
103951tolnaftate 1 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10742-0020-1Mentholatum Heel Revival Cream1 in 1 CARTONCREAM11
10742-0020-1Mentholatum Heel Revival Cream28 g in 1 TUBECREAM281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-0020MENTHOLATUM HEEL REVIVAL CREAM CREAM [THE MENTHOLATUM COMPANY]1Current NDC, 2 package rows20241120_21b643c2-eb6e-8939-e063-6394a90aaeac.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10742-002010742-0020-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mentholatum Heel Revival CreamMENTHOLATUM HEEL REVIVAL CREAMThe Mentholatum Company21b643c2-eb6e-8939-e063-6394a90aaeac2024-09-09WarningsExact identifier
ndc (package): 10742-0020-1
ndc (product): 10742-0020
ndc11 (package): 10742002001
spl id: 21b643c2-eb6f-8939-e063-6394a90aaeac
spl set id: 21b643c2-eb6e-8939-e063-6394a90aaeac

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.