Aspercreme With Lidocaine Foot Pain Cream

Aspercreme With Lidocaine Foot Pain Cream
SPL v6
SPL
SPL Set ID da82cc0e-cc39-408e-87e1-c35bb6f9f51e
Route
TOPICAL
Published
Effective Date 2025-12-19
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Inactive Ingredients
Water Alcohol Cetostearyl Alcohol Ceteth-20 Phosphate Dimethicone Caprylyl Trisiloxane Dihexadecyl Phosphate Glyceryl Monostearate Aloe Vera Leaf Panthenol Alpha-tocopherol Acetate Magnesium Ascorbyl Phosphate Aminomethylpropanol Carbomer Interpolymer Type A (55000 Cps) Ethylhexylglycerin Methylparaben Edetate Disodium Anhydrous Citric Acid Monohydrate

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2018-03-01

Description

ASPERCREME LIDOCAINE FOOT CRE A M Drug Facts


Medication Information

Description

ASPERCREME LIDOCAINE FOOT CRE A M Drug Facts

Use

for the temporary relief of pain

Section 42229-5

ASPERCREME LIDOCAINE FOOT CRE A M

Drug Facts

Warnings

For external use only

Directions

■ adults and children 12 years of age and older:

      ■ apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily

      ■ massage until thoroughly absorbed into skin

      ■ wash hands thoroughly with soap and water after each use

■ children under 12 years of age: ask a doctor

Do Not Use

■ in large quantities

■ on wounds or on irritated or damaged skin

■ with a heating pad

Active Ingredient

Lidocaine HCl 4%

Inactive Ingredients

water, cetearyl alcohol, alcohol denat., ceteth-20 phosphate, dimethicone, caprylyl methicone, dicetyl phosphate, C30-45 alkyl cetearyl dimethicone crosspolymer, triethyl citrate, glyceryl stearate, potassium hydroxide, aloe barbadensis leaf juice, hydroxyacetophenone, fragrance, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, panthenol, tocopheryl acetate, magnesium ascorbyl phosphate

Child-resistant packaging. Close cap tightly after use.

Principal Display Panel

MAX STRENGTH

Aspercreme

WITH 4% LIDOCAINE

PAIN RELIEF CREAM

NET WT 4 OZ (113 g) 

When Using This Product

use only as directed

■ do not bandage tightly

avoid contact with eyes and mucous membranes

do not expose the area to local heat or to direct sunlight

Stop Use and Ask A Doctor If

condition worsens or symptoms persist for more than 7 days

■ symptoms clear up and occur again within a few days

■ redness is present or excessive skin irritation occurs

■ you experience severe burning pain, swelling, or blistering where the product was applied

If Pregnant Or Breast Feeding,

ask a health professional before use.

Keep Out of Reach of Children.

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


Structured Label Content

Use

for the temporary relief of pain

Section 42229-5 (42229-5)

ASPERCREME LIDOCAINE FOOT CRE A M

Drug Facts

Warnings

For external use only

Directions

■ adults and children 12 years of age and older:

      ■ apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily

      ■ massage until thoroughly absorbed into skin

      ■ wash hands thoroughly with soap and water after each use

■ children under 12 years of age: ask a doctor

Do Not Use (Do not use)

■ in large quantities

■ on wounds or on irritated or damaged skin

■ with a heating pad

Active Ingredient (Active ingredient)

Lidocaine HCl 4%

Inactive Ingredients (Inactive ingredients)

water, cetearyl alcohol, alcohol denat., ceteth-20 phosphate, dimethicone, caprylyl methicone, dicetyl phosphate, C30-45 alkyl cetearyl dimethicone crosspolymer, triethyl citrate, glyceryl stearate, potassium hydroxide, aloe barbadensis leaf juice, hydroxyacetophenone, fragrance, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, panthenol, tocopheryl acetate, magnesium ascorbyl phosphate

Child-resistant packaging. Close cap tightly after use.

Principal Display Panel (PRINCIPAL DISPLAY PANEL)

MAX STRENGTH

Aspercreme

WITH 4% LIDOCAINE

PAIN RELIEF CREAM

NET WT 4 OZ (113 g) 

When Using This Product (When using this product)

use only as directed

■ do not bandage tightly

avoid contact with eyes and mucous membranes

do not expose the area to local heat or to direct sunlight

Stop Use and Ask A Doctor If (Stop use and ask a doctor if)

condition worsens or symptoms persist for more than 7 days

■ symptoms clear up and occur again within a few days

■ redness is present or excessive skin irritation occurs

■ you experience severe burning pain, swelling, or blistering where the product was applied

If Pregnant Or Breast Feeding, (If pregnant or breast-feeding,)

ask a health professional before use.

Keep Out of Reach of Children. (Keep out of reach of children.)

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


Advanced Ingredient Data


Raw Label Data

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