Goose Grease Recovery & Pain Relief Cream

Manufacturer
ANC Products LLC
Effective date
2017-02-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:20:07

Label at a glance#

ProductGoose Grease Recovery and Pain Relief
Active ingredientMENTHOL
Label structure6 sections

Dosage and administration

Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age consult a physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

Topical Pain Relief

Indications

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

  • For external use only.
  • Avoid contact with eyes.
  • If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, consult physician.

Do not apply to wounds or damaged skin.

OTC - DO NOT USE SECTION

  • to wounds or damaged skin.
  • Do not bandage tightly

If pregnant or breast feeding.

OTC - PREGNANCY OR BREAST FEEDING SECTION

contact physician prior to use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
  • Children under two-years of age consult a physician.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Achillea millefolium (yarrow) extract, Aloe barbadensis (aloe vera gel) juice, aqua (deionized water), Arnica montana (arnica) extract, beeswax, Bixa orellana (annatto) seed extract, Boswellia serrata extract, Calendula officinalis (marigold) flower extract, caprylic/capric triglyceride, cetearyl olivate, cetyl myristoleate, curcuma longa (turmeric) extract, dimethyl sulfone (msm), emu oil, gluconolactone, glycerin, glyceryl stearate se, Harpagophytum procumbens (devils claw) root extract, Helianthus annuus (sunflower) seed oil, Ilex paraguariensis (yerba mate) leaf extract, magnesium sulfate, Mentha piperita (peppermint) oil, Scutellaria baicalensis (baikal skullcap) root extract, sodium benzoate, sorbitan olivate, stearic acid, tocopheryl acetate (vitamin e), xanthan gum, yucca extract.

Package Lableing:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69896-72869896-728-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
0723fe60-78ea-b7c4-e063-6294a90addedef3eead6-bf7a-4a76-bfee-2a5d5c92946c2023-10-07WarningsExact identifier
spl set id: ef3eead6-bf7a-4a76-bfee-2a5d5c92946c

Reported adverse events (FAERS/openFDA)#

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