GOLD BOND PAIN AND ITCH- benzethonium chloride and lidocaine spray

Gold Bond Pain and Itch by

Drug Labeling and Warnings

Gold Bond Pain and Itch by is a Otc medication manufactured, distributed, or labeled by Chattem, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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)

INGREDIENTS AND APPEARANCE

GOLD BOND PAIN AND ITCH 
benzethonium chloride and lidocaine spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41167-0190
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.2 g  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41167-0190-2	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/02/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	01/02/2017

Labeler - Chattem, Inc. (003336013)