Goose Grease

Dosage form: cream
Ingredients: MENTHOL 12.5mg in 1g
Labeler: ANC Products LLC
NDC code: 69896-020

Medically reviewed by Drugs.com. Last updated on Oct 23, 2023.

Goose Grease

Drug Facts

Active Ingredient

Menthol 1.25%

Purpose

Topical Pain Relief

Indications

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

Warnings

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.

If swallowed, consult physician.

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

If pregnant or breast feeding, contact physician prior to use.

Directions

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

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 (devil's 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.

Product Label

GOOSE GREASE
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69896-020
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (MENTHOL)	MENTHOL	12.5 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL STEARATE SE
HARPAGOPHYTUM PROCUMBENS ROOT
SUNFLOWER OIL
ILEX PARAGUARIENSIS LEAF
MAGNESIUM SULFATE, UNSPECIFIED
PEPPERMINT OIL
SCUTELLARIA BAICALENSIS ROOT
SODIUM BENZOATE
SORBITAN OLIVATE
STEARIC ACID
.ALPHA.-TOCOPHEROL ACETATE
XANTHAN GUM
ACHILLEA MILLEFOLIUM
ALOE VERA LEAF
WATER
ARNICA MONTANA
YELLOW WAX
ANNATTO
INDIAN FRANKINCENSE
CALENDULA OFFICINALIS FLOWER
MEDIUM-CHAIN TRIGLYCERIDES
CETEARYL OLIVATE
CETYL MYRISTOLEATE
TURMERIC
DIMETHYL SULFONE
EMU OIL
GLUCONOLACTONE
GLYCERIN

Packaging
#	Item Code	Package Description
1	NDC:69896-020-01	1 TUBE in 1 CARTON
1		113.4 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/28/2015

Labeler - ANC Products LLC (079844653)

Revised: 10/2019

Document Id: 9639e3a5-4f87-c86c-e053-2995a90a7b27

Set id: a204d1e8-1dd9-49f6-ae46-bb35a39d5d24

Version: 4

Effective Time: 20191031

ANC Products LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer