FDA.reportPublic FDA data

Gold Bond Diabetics Medicated Dry Skin Relief Foot Cream

Manufacturer
Chattem, Inc.
Effective date
2025-03-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:57:38

Label at a glance#

ProductGold Bond Diabetics Medicated Dry Skin Relief Foot Cream
Active ingredientDIMETHICONE, WHITE PETROLATUM
Label structure8 sections

Indications and uses

helps relieve, prevent and temporarily protect chafed, chapped or cracked skin  temporarily protects minor: ■ burns ■ cuts ■ scrapes helps protect from the drying effects of wind and cold weather

Dosage and administration

apply generously to affected area as needed

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts – Gold Bond Diabetics' Medicated Dry Skin Relief Foot Cream

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 3%
White petrolatum 30%

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

  • helps relieve, prevent and temporarily protect chafed, chapped or cracked skin 
  • temporarily protects minor: ■ burns ■ cuts ■ scrapes
  • helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

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

Do not use on

OTC - DO NOT USE SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply generously to affected area as needed

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, glyceryl stearate, distearyldimonium chloride, aloe barbadensis leaf juice, polyethylene, stearyl alcohol, cetearyl alcohol, behentrimonium methosulfate, methyl gluceth-20, steareth-2, steareth-21, allantoin, cetyl alcohol, tocopheryl acetate, butyrospermum parkii (shea) butter extract, PEG-10 phytosterol, polysorbate 60, ceramide NG, stearamidopropyl PGdimonium chloride phosphate, jojoba esters, DMDM hydantoin, magnesium ascorbyl phosphate, butylene glycol, methylparaben, palmitoyl hexapeptide-12, propylene glycol, hydrolyzed jojoba esters, propylparaben, EDTA, potassium hydroxide, tribehenin, C12-15 alkyl benzoate, retinyl palmitate

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gold Bond Diabetics' Medicated Dry Skin Relief Foot Cream
Net wt 3.4 oz (96 g)

PRINCIPAL DISPLAY PANEL Gold Bond Diabetics' Medicated Dry Skin Relief Foot Cream Net wt 3.4 oz (96 g)PRINCIPAL DISPLAY PANEL Gold Bond Diabetics' Medicated Dry Skin Relief Foot Cream Net wt 3.4 oz (96 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1042645dimethicone 3 % / petrolatum 30 % Topical CreamPSN1
1042645dimethicone 30 MG/ML / petrolatum 300 MG/ML Topical CreamSCD1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41167-0541-0Gold Bond Diabetics Medicated Dry Skin Relief Foot Cream1 in 1 CARTONCREAM11
41167-0541-0Gold Bond Diabetics Medicated Dry Skin Relief Foot Cream96 g in 1 TUBECREAM961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41167-0541GOLD BOND DIABETICS MEDICATED DRY SKIN RELIEF FOOT CREAM (DIMETHICONE, WHITE PETROLATUM) CREAM [CHATTEM, INC.]1Current NDC, 2 package rows20250323_b951d1cb-b81e-4d7f-9a67-8405daa89667.zip

Products#

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

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41167-054141167-0541-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OACTIB
WHITE PETROLATUMB6E5W8RQJ4ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL STEARATE230OU9XXE4IACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
POLYETHYLENEUG00KM4WR7IACT
STEARYL ALCOHOL2KR89I4H1YIACT
CETEARYL ALCOHOL2DMT128M1SIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
METHYL GLUCETH-20J3QD0LD11PIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
ALLANTOIN344S277G0ZIACT
CETYL ALCOHOL936JST6JCNIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
POLYSORBATE 60CAL22UVI4MIACT
CERAMIDE NGC04977SRJ5IACT
STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEW6000VEI5YIACT
DMDM HYDANTOINBYR0546TOWIACT
MAGNESIUM ASCORBYL PHOSPHATE0R822556M5IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
METHYLPARABENA2I8C7HI9TIACT
PALMITOYL HEXAPEPTIDE-12HO4ZT5S86CIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
HYDROLYZED JOJOBA ESTERSUDR641JW8WIACT
PROPYLPARABENZ8IX2SC1OHIACT
EDTA9G34HU7RV0IACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
TRIBEHENIN8OC9U7TQZ0IACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
RETINYL PALMITATE1D1K0N0VVCIACT
JOJOBA OIL, RANDOMIZED7F0EV20QYLIACT

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
Gold Bond Diabetics Medicated Dry Skin Relief Foot CreamDIMETHICONE, WHITE PETROLATUMChattem, Inc.b951d1cb-b81e-4d7f-9a67-8405daa896672025-03-19WarningsExact identifier
ndc (package): 41167-0541-0
ndc (product): 41167-0541
ndc11 (package): 41167054100
spl id: 3c5f7559-402a-4bf3-90d3-a5ac7242cf75
spl set id: b951d1cb-b81e-4d7f-9a67-8405daa89667

Reported adverse events (FAERS/openFDA)#

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