Meijer Ultra Strength Pain Relieving Cream

Manufacturer
MEIJER, INC.
Effective date
2022-03-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:04:36

Label at a glance#

ProductMeijer Ultra Strength Pain Relieving Cream
Active ingredientMETHYL SALICYLATE, MENTHOL, UNSPECIFIED FORM, CAMPHOR (SYNTHETIC)
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purposes

Camphor 4%...................................Topical analgesic

Menthol 10%...................................Topical analgesic

Methyl salicylate 30%......................Topical analgesic

OTC - PURPOSE SECTION

Uses

temporarily relieves the minor aches and pains of muscles and joints associated with:

  • sprains
  • simple backache
  • arthritis
  • strains
  • bruises

WARNINGS SECTION

Warnings

For external use only

Allergy alert

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age with arthritis-like conditions

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have redness over the affected area.

OTC - WHEN USING SECTION

When using this product

  • do not use otherwise than as directed
  • avoid contact with eyes, mucous membranes or rashes
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • redness is present or irritation or rash develops
  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, 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 (1-800-222-1222) right away.

INDICATIONS & USAGE SECTION

Directions

  • use only as directed
  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: ask a doctor

DOSAGE & ADMINISTRATION SECTION

Other Information

  • store at room temperature 20-25ºC (68-77ºF)

INACTIVE INGREDIENT SECTION

Inactive ingredients

ethylparaben, glyceryl monostearate, polysorbate 80, purified water, sorbitan monooleate, stearic acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2535025350

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79481-822779481-8227-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
efe788d9-6658-6232-e053-2a95a90a7bbca9f28d36-7edc-44ca-e053-2995a90a82fd2022-12-15WarningsExact identifier
spl set id: a9f28d36-7edc-44ca-e053-2995a90a82fd

Reported adverse events (FAERS/openFDA)#

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