GOLD ICE PAIN RELIEF- menthol cream

GOLD ICE Pain Relief by

Drug Labeling and Warnings

GOLD ICE Pain Relief by is a Otc medication manufactured, distributed, or labeled by Eden's Answers, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 6.25%

Purpose

External Analgesic

Uses

temporary relief of minor aches and pains of muscles and joints associated with: 

• simple backache 
• arthritis
• strains
• bruises
• sprains

Warnings:

For external use only

Keep away from fire or flame Flammable:

When using this product

• do not apply to wounds or damaged skin
• Do not bandage tightly
• do not use with a heating pad
• avoid contact with the eyes or mucous membranes 
• use only as directed

Stop Use and ask a Doctor if

• condition worsens
• symptoms persist for more than 7 days or clears up and occur again within a few days.
• redness or skin irritation occurs

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply to affected area not more than 3 to 4 times daily Adult and children 12 years of age and over:

consult a physician Children under 12 years of age:

Other information

• close container tightly and store at room temperature 
• do not use if plastic seal around cap is broken or missing
• store in a cool, dry place

Inactive Ingrediets

Beeswax, Capsicum Frutescens Fruit Powder, Lavandula Angustifolia (Lavender) Flower Extract, Lavandulaangustifolia (lavender) Oil, Mentha Piperita (Peppermint) Leaf, Rosmarinus officinalis (Rosemary) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Oil, Verbascum Thapsus Extract

Questions or Comments?

Sprigs Life Inc PO Box 387 

Millersburg, Ohio 44654 1-888-990-7763

Mon-Fri 8am-3pm EST

Package Labeling:

INGREDIENTS AND APPEARANCE

GOLD ICE PAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72226-305
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	62.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
YELLOW WAX (UNII: 2ZA36H0S2V)
TABASCO PEPPER (UNII: J1M3NA843L)
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
LAVENDER OIL (UNII: ZBP1YXW0H8)
MENTHA PIPERITA LEAF (UNII: A389O33LX6)
ROSEMARY (UNII: IJ67X351P9)
ROSEMARY OIL (UNII: 8LGU7VM393)
VERBASCUM THAPSUS WHOLE (UNII: C9TD27U172)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72226-305-00	1 in 1 BOX	08/01/2020
1		100 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/01/2020

Labeler - Eden's Answers, Inc. (030063091)