GOLD BOND ORIGINAL STRENGTH- menthol powder GOLD BOND EXTRA STRENGTH- menthol powder

Gold Bond by

Drug Labeling and Warnings

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

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Gold Bond Medicated Original Strength Body Powder

Drug Facts

Active ingredient

Menthol 0.15%

Purpose

Anti-Itch

Uses

temporarily relieves the pain and itch associated with:

• minor cuts
  
• sunburn
  
• insect bites
  
• scrapes
  
• minor burns
  
• minor skin irritations

Warnings

For external use only

When using this product

• 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
  
• redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

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

Directions

• adults and children 2 years and older: apply freely up to 3 or 4 times daily 
  
• children under 2 years: ask a doctor
  
• for best results dry skin thoroughly before applying

Inactive ingredients

talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-004)

Gold Bond Medicated Extra Strength Body Powder

Drug Facts

Active ingredient

Menthol 0.8%

Purpose

Anti-Itch

Uses

temporarily relieves the pain and itch associated with:

• minor cuts
  
• sunburn
  
• insect bites
  
• scrapes
  
• minor burns
  
• minor skin irritations

Warnings

For external use only

When using this product

• 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
  
• redness, irritation, swelling or pain persists or increases

Keep out of reach of children.

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

Directions

• adults and children 2 years and older: apply freely up to 3 or 4 times daily 
  
• children under 2 years: ask a doctor
  
• for best results dry skin thoroughly before applying

Inactive ingredients

talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-006)

PRINCIPAL DISPLAY PANEL

Gold Bond
Medicated Healing Since 1908

Original Strength

BODY POWDER
Triple Action Relief
Cooling ● Absorbing ● Itch Relieving

Menthol 0.15%
Net wt 4 oz (113 g)

PRINCIPAL DISPLAY PANEL

Gold Bond
Healing Medicated Since 1908
Extra Strength

BODY POWDER

Triple Action Relief
Cooling ● Absorbing ● Itch Relieving

Menthol 0.8%
Net wt 4 oz (113 g)

INGREDIENTS AND APPEARANCE

GOLD BOND  ORIGINAL STRENGTH
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41167-0104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.0015 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
ZINC OXIDE (UNII: SOI2LOH54Z)
ACACIA (UNII: 5C5403N26O)
EUCALYPTOL (UNII: RV6J6604TK)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
ZINC STEARATE (UNII: H92E6QA4FV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41167-0104-0	113 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996
2	NDC: 41167-0104-1	28 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996
3	NDC: 41167-0104-3	283 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996
4	NDC: 41167-0104-6	679 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	04/29/1996

GOLD BOND  EXTRA STRENGTH
menthol powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41167-0404
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.008 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TALC (UNII: 7SEV7J4R1U)
ZINC OXIDE (UNII: SOI2LOH54Z)
ACACIA (UNII: 5C5403N26O)
EUCALYPTOL (UNII: RV6J6604TK)
METHYL SALICYLATE (UNII: LAV5U5022Y)
SALICYLIC ACID (UNII: O414PZ4LPZ)
THYMOL (UNII: 3J50XA376E)
ZINC STEARATE (UNII: H92E6QA4FV)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41167-0404-0	113 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996
2	NDC: 41167-0404-1	283 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/1996

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	04/29/1996

Labeler - Chattem, Inc. (003336013)