FDA.reportPublic FDA data

Gold Bond Medicated Original Strength Lotion

Manufacturer
Chattem, Inc.
Effective date
2016-03-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:15:36

Label at a glance#

ProductGold Bond Original Medicated
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

temporarily relieves the pain and itching associated with: minor skin irritations minor burns minor cuts insect bites sunburn scrapes

Dosage and administration

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts - Original Strength Gold Bond Body Lotion

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15%

Purpose

OTC - PURPOSE SECTION

Anti-itch

Uses

INDICATIONS & USAGE SECTION

temporarily relieves the pain and itching associated with:

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

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41167-061141167-0611-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERINPDC6A3C0OXIACT
PETROLATUM4T6H12BN9UIACT
ALOE VERA LEAFZY81Z83H0XIACT
CETYL ALCOHOL936JST6JCNIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEW6000VEI5YIACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
STEARETH-2V56DFE46J5IACT
POLYSORBATE 60CAL22UVI4MIACT
STEARETH-2153J3F32P58IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
EDETATE DISODIUM7FLD91C86KIACT
IMIDUREAM629807ATLIACT
METHYLPARABENA2I8C7HI9TIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
df12012c-9cec-42f8-9b91-4eccbbb95d220381fad4-e43f-4a1b-b27f-d94a269e5e092023-01-05WarningsExact identifier
spl set id: 0381fad4-e43f-4a1b-b27f-d94a269e5e09

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.