OTC Medication Information: Goose Grease

GOOSE GREASE- menthol cream
ANC Products LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

Box
(click image for full-size original)

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 Multilevel Packaging
1 NDC:69896-020-01 1 TUBE in 1 CARTON contains a TUBE
1 113.4 g in 1 TUBE This package is contained within the CARTON (69896-020-01)
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 ANC Products LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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