blue goo Pain Relieving Cream

Label at a glance#

Contacts and useful links#

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Methyl Salicylate 15%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Topical analgesic

Use(s)

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints; associated with simple backache, arthritis, strains, bruises, and sprains.

Warnings

WARNINGS SECTION

For external use only

SPL UNCLASSIFIED SECTION

For external use only.

ALLERGY ALERT

SPL UNCLASSIFIED SECTION

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

When using this product

OTC - WHEN USING SECTION

•Avoid contact with eyes

•Use only as directed

•Perform a patch test prior to use. A transient burning sensation may occur upon application. With regular use, this sensation generally disappears after several days.

•Do not apply to wounds or damaged skin

•Do not bandage tightly 

•Do not use with a heating pad.

Stop use and ask a doctor if

OTC - STOP USE SECTION

•severe burning persists or blistering occurs

•condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Pregnancy/Breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding ask a health professional before use.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 6 years of age: consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

allantoin, aloe barbadensis leaf juice, benzyl alcohol, carbomer, ceteareth-20, cetearyl alcohol, cetyl alcohol, dimethicone, dimethyl sulfone, emu oil, fragrance, glucosamine HCl, panthenol, phenoxyethanol, polysorbate 20, red 33, sodium chondroitin sulfate, sodium hydroxide, stearic acid, water, zingiber officinale (ginger) root extract.

Questions

OTC - QUESTIONS SECTION

Questions or comments? 1-866-567-8600

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EXTRA STRENGTH

DEEP HEATING RUB

blue goo

Pain

RELIEVING 

Cream

WITH 100% PURE EMU OIL

HELPS TO RELIEVE:

•Aches & Pains from Muscles & Joints

Associated with:

•Backaches •Arthritis •Sprains

•Neckaches •Stiff Joints •Strains

Use before activity to loosen muscles and allow for greater movement and flexibility

NET WT 32 OZ (907 g)

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

• Pain Relieving Cream Analgesic
• Menthol, Unspecified Form and Methyl Salicylate
• MENTHOL
• METHYL SALICYLATE 2-ETHYLBUTYRATE
• ALLANTOIN
• ALOE BARBADENSIS LEAF JUICE
• BENZYL ALCOHOL
• CARBOMER
• CETEARETH-20
• CETEARYL ALCOHOL
• CETYL ALCOHOL
• DIMETHICONE
• DIMETHYL SULFONE
• EMU OIL
• FRAGRANCE 13576
• GLUCOSAMINE HCL
• PANTHENOL
• PHENOXYETHANOL
• POLYSORBATE 20
• RED 33
• SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW)
• SODIUM HYDROXIDE
• STEARIC ACID
• WATER
• ZINGIBER OFFICINALE (GINGER) ROOT OIL

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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.

Reported adverse events (FAERS/openFDA)#

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