FDA.reportPublic FDA data

Conquer Pain Relief Cream

Manufacturer
Steuart Contract Packaging
Effective date
2022-09-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:53:46

Label at a glance#

ProductConquer Pain Relief Cream
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains associated with arthritis simple backache strains bruises sprains

Dosage and administration

shake well apply to affected area not more than 4 times daily massage painful area until absorbed into skin wash hands after each use with cold water Children under 12 years of age: consult a doctor

Storage and handling

store in a cool place away from direct sunlight store with lid closed tightly

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains associated with

  • arthritis
  • simple backache
  • strains
  • bruises
  • sprains

Warning

WARNINGS SECTION

For external use only

Flammable: Keep away from fire or flame and heated surfaces

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any ingredient
  • on open wounds, damaged, or irritated skin
  • with a heating pad or TENS device
  • after expiration date

When using this product

OTC - WHEN USING SECTION

  • do not bandage tightly
  • use only as directed
  • avoid contact with eyes or mucous

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • rash, itching, redness or excessive irritation on the skin develops
  • symptoms last more than 7 days
  • symptoms clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions for adults and children 12 years of age and over

DOSAGE & ADMINISTRATION SECTION

  • shake well
  • apply to affected area not more than 4 times daily
  • massage painful area until absorbed into skin
  • wash hands after each use with cold water

Children under 12 years of age: consult a doctor

Other Information

STORAGE AND HANDLING SECTION

  • store in a cool place away from direct sunlight
  • store with lid closed tightly

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis Leaf (Aloe Vera) Juice, Arnica Montana Flower Extract, Carbomer, Carthamus tinctorious (Safflower) Seed Oil, Cetyl Alcohol, Deionized Water, Dimethyl Sulfone, Ethylhexylglycerin, Glucosamine Sulfate - Glucosamine Sulfate Potassium Chloride, Glycerin, Hemp Extract, Hempseed Oil, Olea europaea (Olive) Oil, Phenoxyethanol, Polysorbate 20, Salix alba, Phenoxyethanol, Polysorbate 20, Salix alba (Willow) Bark Extract, Symphytum Officinale (Comfrey) Leaf Extract

PRINCIPAL DISPLAY PANEL - 3.4 oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CREATED BY PAIN RELIEF EXPERTS

CONQUER
PAIN

MAX STRENGTH

NEUROPATHY
PAIN CREAM

ARNICA | HEMP EXTRACT | MENTHOL | ALOE

PROFESSIONALLY
FORMULATED

FAST RELIEF

INCREASE BLOOD
CIRCULATION

INSTANT
ABSORPTION

70%
MORE
PRODUCT
THAN 2 OZ

MADE IN
THE USA

Net WT 3.4 oz

PRINCIPAL DISPLAY PANEL - 3.4 oz Bottle Label
PRINCIPAL DISPLAY PANEL - 3.4 oz Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63374-034-012024-10-22C16284748780-11030e365-03e9-111a-e063-dadaa90a10e2Conquer Pain Relief Cream
63374-034-012024-01-30C16284748780-11030e365-03e9-111a-e063-dadaa90a10e2Conquer Pain Relief Cream

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63374-03463374-034-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
SALIX ALBA BARK205MXS71H7IACT
COMFREY LEAFDG4F8T839XIACT
SAFFLOWER OIL65UEH262ISIACT
Water059QF0KO0RIACT
OLIVE OIL6UYK2W1W1EIACT
EDETATE SODIUMMP1J8420LUIACT
ALOE VERA LEAFZY81Z83H0XIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TROLAMINE9O3K93S3TKIACT
POLYSORBATE 207T1F30V5YHIACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
GLYCERINPDC6A3C0OXIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CETYL ALCOHOL936JST6JCNIACT

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
b33caeda-6301-49d8-9b36-1c9597f4b4bab49664d5-e722-4790-92a0-c0e8b95529342024-10-22WarningsExact identifier
spl set id: b49664d5-e722-4790-92a0-c0e8b9552934

Reported adverse events (FAERS/openFDA)#

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