Aspercreme Lidocaine Foot Cream-Diabetic

Manufacturer
Chattem, Inc.
Effective date
2026-01-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
monthly-update
Hydrated at
2026-06-03 17:52:35

Label at a glance#

ProductAspercreme Lidocaine Foot (Diabetic)
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Dosage and administration

adults and children over 12 years: ■ apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period ■ massage into painful area until thoroughly absorbed into skin          children 12 years or younger :  ask a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

ASPERCREME with LIDOCAINE FOOT PAIN CREAM

(For Diabetic Skin)

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Use

INDICATIONS & USAGE SECTION

temporarily relieves minor pain

Warnings

WARNINGS SECTION

For external use only 

Do not use

OTC - DO NOT USE SECTION

■ if you have serious foot problems, such as ulcers or infections 

■ if you have numbness or reduced ability to feel pain

■ on cut, irritated or swollen skin

■on puncture wounds

■ for more than one week without consulting a doctor

When using this product

OTC - WHEN USING SECTION

■ use only as directed. Read and follow all directions and warning on this carton.

■ do not allow contact with the eyes and the mucous membranes

■ do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use

■ do not use at the same time as other topical analgesics

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens 

■ redness is present

■ irritation develops

■ symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years:

■ apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period

■ massage into painful area until thoroughly absorbed into skin

        

children 12 years or younger: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, alcohol denat. (10%), cetearyl alcohol, ceteth-20 phosphate, dimethicone, caprylyl methicone, dicetyl phosphate, glyceryl stearate, aloe barbadensis leaf juice, panthenol, tocopheryl acetate, magnesium ascorbyl phosphate, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, methylparaben, disodium EDTA, citric acid

                                                                                    333-105

Child-resistant packaging. Close cap tightly after use.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Max Strength
Aspercreme

Lidocaine

2 in 1

Pain Relief + Moisturization

foot cream

PRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot creamPRINCIPAL DISPLAY PANEL Max Strength Aspercreme Lidocaine 2 in 1 Pain Relief + Moisturization foot cream

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1010895lidocaine HCl 4 % Topical CreamPSN4
1010895lidocaine hydrochloride 40 MG/ML Topical CreamSCD4
1010895lidocaine hydrochloride 4 % Topical CreamSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41167-0597-0Aspercreme Lidocaine Foot (Diabetic)1 in 1 CARTONCREAM14
41167-0597-0Aspercreme Lidocaine Foot (Diabetic)113 g in 1 BOTTLE, PLASTICCREAM1134

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41167-059741167-0597-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32023-10-23full-release2026-05-31 23:57:06

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
Aspercreme Lidocaine Foot (Diabetic)LIDOCAINE HYDROCHLORIDEChattem, Inc.2c33d15e-5032-46d9-bd98-5abc7df3bbe52026-01-13WarningsExact identifier
ndc (package): 41167-0597-0
ndc (product): 41167-0597
ndc11 (package): 41167059700
spl id: 6e841df3-1b00-4aad-88d9-23844eb8891e
spl set id: 2c33d15e-5032-46d9-bd98-5abc7df3bbe5

Reported adverse events (FAERS/openFDA)#

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