GOLD BOND EXTRA STRENGTH- menthol lotion 
Chattem, Inc.

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Gold Bond Medicated Extra Strength Lotion

Drug Facts – Extra Strength Gold Bond Body Lotion

Active ingredients

Menthol 0.5%

Purpose

Anti-itch

Uses

temporarily relieves the pain and itching associated with:

Warnings

For external use only

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns
  • large areas of the body

When using this product

  • do not get into eyes or nose
  • not for prolonged use

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 right away.

Directions

adults and children 2 years and older: apply to affected area up to 3 or 4 times daily

children under 2 years: ask a doctor

Inactive ingredients

water, dimethicone, glycerin, petrolatum, aloe barbadensis leaf juice, cetyl alcohol, stearyl alcohol, propylene glycol, stearamidopropyl PG-dimonium chloride phosphate, distearyldimonium chloride, cetearyl alcohol, polysorbate 60, steareth-21, steareth-2, tocopheryl acetate, EDTA, imidazolidinyl urea, methylparaben, potassium hydroxide, fragrance

PRINCIPAL DISPLAY PANEL

GOLD BOND® 
EXTRA STRENGTH
BODY LOTION
Triple Action Relief
For Extra Dry & Itchy Skin
Net wt 14 oz (396 g)

GOLD BOND® 
EXTRA STRENGTH
BODY LOTION
Triple Action Relief 
For Extra Dry & Itchy Skin
Net wt 14 oz (396 g)

GOLD BOND EXTRA STRENGTH 
menthol lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0641
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.005 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
PETROLATUM (UNII: 4T6H12BN9U)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)  
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
STEARETH-21 (UNII: 53J3F32P58)  
STEARETH-2 (UNII: V56DFE46J5)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
IMIDUREA (UNII: M629807ATL)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0641-2396 g in 1 BOTTLE; Type 0: Not a Combination Product03/11/2016
2NDC:41167-0641-4476 g in 1 BOTTLE; Type 0: Not a Combination Product03/11/201609/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/11/2016
Labeler - Chattem, Inc. (003336013)

Revised: 10/2023
Document Id: ce3d0863-716d-4e90-b3c9-d90183bf0f28
Set id: 98ea15e6-972f-44a3-a1e4-abeae538d5a7
Version: 5
Effective Time: 20231030
 
Chattem, Inc.