Foot Works
- Manufacturer
- Avon Products, Inc.
- Effective date
- 2012-05-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:32:09
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Benzalkonium Chloride 0.13%.......
Lidocaine 2%.........
OTC - PURPOSE SECTION
Purpose
........First aid antiseptic
...........External analgesic
INDICATIONS & USAGE SECTION
Uses
• first aid to help reduce the risk of skin infection in minor cuts, scrapes and burns
• first aid for the temporary relief of pain in minor cuts, scrapes and burns
WARNINGS SECTION
Warnings
For external use only
• do not use in the eyes or apply over large areas of the body
• do not use in large quantities, particularly over raw surfaces or blistered areas
• consult a doctor in the case of deep or puncture wounds, animal bites, or serious burns
• if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
Adults and children 2 years of age and older:
• clean the affected area
• apply a small amount of this product on the affected area 1 to 3 times daily
• may be covered with a sterile bandage
Children under 2 years of age:
• consult a doctor
INACTIVE INGREDIENT SECTION
Inactive ingredients
WATER/EAU, ISOPROPYL PALMITATE, STEARYL ALCOHOL, CETYL ALCOHOL, GLYCERYL STEARATE SE, UREA, CANOLA OIL/HUILE DE COLZA, DIMETHICONE, TRIETHANOLAMINE, POLYSORBATE 80, BENZYL ALCOHOL, LACTIC ACID, ALLANTOIN, METHYLPARABEN, SD ALCOHOL 40-B.
OTC - QUESTIONS SECTION
Questions? Call 1-800-FOR-AVON or 1-800-265-AVON in Canada
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| LIDOCAINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 10096-4423-1 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bef1-f6ea-e053-dbdaa90aa703 | Drug Facts |
| 10096-4423-2 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bef1-f6ea-e053-dbdaa90aa703 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10096-4423-1 | Foot WorksCracked Heel | 50 mL in 1 TUBE | CREAM | 50 | 1 | |
| 10096-4423-2 | Foot WorksCracked Heel | 75 mL in 1 TUBE | CREAM | 75 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10096-4423 | FOOT WORKS CRACKED HEEL (LIDOCAINE, BENZALKONIUM CHLORIDE ) CREAM [AVON PRODUCTS, INC.] | 1 | Legacy NDC, 2 package rows | 20120531_b03b24ce-0790-4b79-ae7c-d2e734e18472.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BENZALKONIUM CHLORIDE | ACTIVE INGREDIENT | F5UM2KM3W7 | 1 | |
| LIDOCAINE | ACTIVE INGREDIENT | 98PI200987 | 1 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | 1 | |
| LIDOCAINE | ACTIVE MOIETY | 98PI200987 | 1 |
Products#
Every source-derived product name is available through these pages.
- Foot Works Cracked Heel
- Lidocaine, BENZALKONIUM CHLORIDE
- LIDOCAINE
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10096-4423 | 10096-4423-1, 10096-4423-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LIDOCAINE | 98PI200987 | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| d16052fb-5197-4680-b1fa-6dc03084fc53 | b03b24ce-0790-4b79-ae7c-d2e734e18472 | 2012-05-30 | Warnings | d16052fb-5197-4680-b1fa-6dc03084fc53 b03b24ce-0790-4b79-ae7c-d2e734e18472 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.



