GOLD BOND PAIN AND ITCH- benzethonium chloride and lidocaine spray 
Chattem, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Gold Bond Pain and Itch Spray

Drug Facts

Active ingredient

Benzethonium chloride 0.2%
Lidocaine HCl 4%

Purpose

First aid antiseptic
Topical anesthetic

Uses

first aid to help protect against infection and for the temporary relief of pain and itching in:

  • minor cuts
  • scrapes
  • burns

Warnings

For external use only

  • Avoid spraying in eyes or on mucous membranes.

Do not use

  • in large quantities, particularly over raw surfaces or blistered areas
  • in eyes or apply over large areas of the body

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

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.

Directions

adults and children 12 years and older:

  • clean the affected area
  • spray a small amount of this product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

children under 12 years of age: consult a doctor

Other information

Store at room temperature 15º-30ºC (59º-86ºF)

Inactive ingredients

4-t-butylcyclohexanol, aloe barbadensis leaf juice, avena sativa (oat) kernel extract, disodium EDTA, ethoxydiglycol, ethylhexylglycerin, glycerin, methyl gluceth-20, pentylene glycol, potassium hydroxide, propanediol, SD alcohol 40 (15%), water

PRINCIPAL DISPLAY PANEL

GOLD BOND
LIDOCAINE + BENZETHONIUM CHLORIDE
PAIN & ITCH RELIEF
ANTISEPTIC SPRAY
2 fl oz (59 mL)

GOLD BOND LIDOCAINE + BENZETHONIUM CHLORIDE PAIN & ITCH RELIEF ANTISEPTIC SPRAY 2 fl oz (59 mL)

GOLD BOND PAIN AND ITCH 
benzethonium chloride and lidocaine spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0190
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.2 g  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
4-TERT-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
OAT (UNII: Z6J799EAJK)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
PROPANEDIOL (UNII: 5965N8W85T)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0190-259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/02/201712/28/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34801/02/201712/28/2020
Labeler - Chattem, Inc. (003336013)

Revised: 1/2016
Document Id: e8fce759-5d6b-4adc-804d-3fd2381be34c
Set id: 2cf83b23-4614-4c80-ad9f-f6b10bdae9ed
Version: 2
Effective Time: 20160115
 
Chattem, Inc.