GOLD BOND MEDICATED PAIN AND ITCH RELIEF- lidocaine hydrochloride cream 
Chattem, Inc.

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Gold Bond Medicated Pain and Itch Relief

Gold Bond® Medicated
Pain & Itch Relief Cream with Lidocaine

Drug Facts

Active ingredient

Lidocaine HCl 4%

Purpose

Topical anesthetic

Use

for temporary relief of the pain and itching associated with:

Warnings

For external use only

Do not use

  • in large quantities, particularly over raw surfaces of blistered area
  • on deep or puncture wounds

When using this product

  • use only as directed. Read and follow all directions and warnings on this carton.
  • avoid contact with eyes

Stop use and ask a doctor if

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

Keep out of reach of children.

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

Directions

adults and children 12 years of age and older:

children under 12 years of age: consult a doctor

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, 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, SD alcohol 40 (15%), steareth-21, water (309-179)

Child resistant packaging. Close cap tightly between uses.

PRINCIPAL DISPLAY PANEL

GoldBond
Pain & Itch Relief Cream
Net Wt 1.75 oz (49g)

PRINCIPAL DISPLAY PANEL
GoldBond
Pain & Itch Relief Cream
Net Wt 1.75 oz (49g)

GOLD BOND MEDICATED PAIN AND ITCH RELIEF 
lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0505
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETETH-20 PHOSPHATE (UNII: 921FTA1500)  
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ALCOHOL (UNII: 3K9958V90M)  
STEARETH-21 (UNII: 53J3F32P58)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0505-01 in 1 CARTON01/15/2016
149 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/15/2016
Labeler - Chattem, Inc. (003336013)

Revised: 10/2023
Document Id: c1b8f43f-1db9-4659-a56a-0daf59d3baef
Set id: 0a2daa61-026f-4d1a-a2ec-6d660ab8f30e
Version: 3
Effective Time: 20231030
 
Chattem, Inc.