GOLD BOND MAXIMUM STRENGTH FOOT PAIN RELIEF- lidocaine hydrochloride cream

Gold Bond Maximum Strength Foot Pain Relief by

Drug Labeling and Warnings

Gold Bond Maximum Strength Foot Pain Relief by is a Otc medication manufactured, distributed, or labeled by Gold Bond Co LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Gold Bond®   Maximum Strength Foot Pain
Relief Cream with Lidocaine

Drug Facts

Active ingredient

Lidocaine HCl 4%

Purpose

Topical anesthetic

Use

Temporarily relieves minor pain   

Warnings

For external use only

Do not use

• 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

• use only as directed. Read and follow all directions and warnings on this carton.
  
• avoid contact with eyes and 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 same time as other topical analgesics

Stop use and ask a doctor if

• 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,

ask a health professional before use.

Keep out of reach of children.

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

Directions

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 under 12 years of age: ask a doctor

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat. (15%), aloe barbadensis leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glyceryl stearate, methylparaben, steareth-21, water 

Child resistant packaging. Close cap tightly after use.

PRINCIPAL DISPLAY PANEL

Gold Bond Maximum Strength Foot Pain Relief Cream
Net Wt 1.75 oz (49g)

INGREDIENTS AND APPEARANCE

GOLD BOND MAXIMUM STRENGTH FOOT PAIN RELIEF 
lidocaine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84714-0427
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
CAPRYLYL METHICONE (UNII: Q95M2P1KJL)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
DICETYL PHOSPHATE (UNII: 2V6E5WN99N)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
STEARETH-21 (UNII: 53J3F32P58)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84714-0427-6	1 in 1 CARTON	03/01/2026
1		49 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2026

Labeler - Gold Bond Co LLC (119184861)