FDA.reportPublic FDA data

Gold Bond Intensive Relief Anti-Itch

Manufacturer
Chattem, Inc.
Effective date
2026-01-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:32:48

Label at a glance#

ProductGold Bond Intensive Relief Anti-Itch
Active ingredientPRAMOXINE HYDROCHLORIDE, MENTHOL
Label structure8 sections

Dosage and administration

adults and children 2 years of age and older :   apply freely to affected area not more than 3 to 4 times daily children under 2 years of age : consult a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

GOLD BOND® Medicated

Intensive Relief Anti-Itch Lotion

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.5%
Pramoxine hydrochloride 1%

Purpose

OTC - PURPOSE SECTION

Anti-itch
Anti-itch

Use

INDICATIONS & USAGE SECTION

for temporary relief of pain and itching associated with:

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

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

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

adults and children 2 years of age and older: apply freely to affected area not more than 3 to 4 times daily

children under 2 years of age: consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, dimethicone, cetyl alcohol, petrolatum, distearyldimonium chloride, aloe barbadensis leaf juice, glyceryl stearate, stearyl alcohol, cetearyl alcohol, behentrimonium methosulfate, steareth-21, propylene glycol, polysorbate 60, stearamidopropyl PG-dimonium chloride phosphate, diazolidinyl urea, butylene glycol, tocopheryl acetate, potassium hydroxide, methylparaben, panthenol, ethoxydiglycol, EDTA, avena sativa (oat) kernel extract

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOLD BOND
ANTI-ITCH LOTION
INTENSIVE RELIEF
Net wt 5.5 oz (155 g)

GOLD BOND ANTI-ITCH LOTION INTENSIVE RELIEF Net wt 5.5 oz (155 g)GOLD BOND ANTI-ITCH LOTION INTENSIVE RELIEF Net wt 5.5 oz (155 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1293905menthol 0.5 % / pramoxine HCl 1 % Topical LotionPSN4
1293905menthol 5 MG/ML / pramoxine hydrochloride 10 MG/ML Topical LotionSCD4
1293905menthol 0.5 % / pramoxine hydrochloride 1 % Topical LotionSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix823511-01gold-bond-intensive-relief-anti-itch-01.jpg
Data codeData Matrix823512-01gold-bond-intensive-relief-anti-itch-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41167-0507-0Gold Bond Intensive Relief Anti-Itch155 g in 1 BOTTLELOTION1554

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41167-050741167-0507-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
PRAMOXINE HYDROCHLORIDE88AYB867L5ACTIB
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
DIMETHICONE92RU3N3Y1OIACT
CETYL ALCOHOL936JST6JCNIACT
PETROLATUM4T6H12BN9UIACT
DISTEARYLDIMONIUM CHLORIDEOM9573ZX3XIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
STEARYL ALCOHOL2KR89I4H1YIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
STEARETH-2153J3F32P58IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYSORBATE 60CAL22UVI4MIACT
STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEW6000VEI5YIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
METHYLPARABENA2I8C7HI9TIACT
PANTHENOLWV9CM0O67ZIACT
DIETHYLENE GLYCOL MONOETHYL ETHERA1A1I8X02BIACT
EDETIC ACID9G34HU7RV0IACT
OATZ6J799EAJKIACT

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 Intensive Relief Anti-ItchPRAMOXINE HYDROCHLORIDE, MENTHOLChattem, Inc.e5a3f8d4-b3d8-4b88-b9a9-833406d3e6f82026-01-14WarningsExact identifier
ndc (package): 41167-0507-0
ndc (product): 41167-0507
ndc11 (package): 41167050700
spl id: 081ef785-fe00-4339-8aa6-c93b44f076e8
spl set id: e5a3f8d4-b3d8-4b88-b9a9-833406d3e6f8

Reported adverse events (FAERS/openFDA)#

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