Up and Up Ultra Strength Pain Relieving Cream

Manufacturer
Target Corporation
Effective date
2018-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:44:58

Label at a glance#

ProductUp and Up Ultra Strength Pain Relieving
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure7 sections

Indications and uses

the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains helps to temporarily relieve minor aches, joint discomfort and muscle pain.

Dosage and administration

Adults and children over 12 years apply to affected area no more than 3-4 times daily Children 12 years or younger: ask a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor, 4%

Menthol, 10%

Methyl Salicylate, 30%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains helps to temporarily relieve minor aches, joint discomfort and muscle pain.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • other than as directed
  • with a heating pad (may blister skin)
  • on children under 12 years of age

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes or mucous membranes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

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
  • skin redness or excessive irritation of the skin develops.

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 over 12 years
  • apply to affected area no more than 3-4 times daily
  • Children 12 years or younger: ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

  • store at 20-25 C (68-77 F)
  • Lot # & Exp. date: see crimp of tube or see box

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, edetate disodium, glyceryl stearate, lanolin, PEG-100 stearate, polysorbate 80, potassium hydroxide, purified water, stearic acid, trolamine.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel2Label2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-96011673-960-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
fe25b91e-4c27-07a1-e053-6394a90a20d91ac4d52c-8515-487d-a6a8-9de6f5e16c732023-06-15WarningsExact identifier
spl set id: 1ac4d52c-8515-487d-a6a8-9de6f5e16c73

Reported adverse events (FAERS/openFDA)#

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