Label: GOLD ICE PAIN RELIEF- menthol cream
- NDC Code(s): 72226-305-00
- Packager: Eden's Answers, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
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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
- Directions
- Other information
- Inactive Ingrediets
- Questions or Comments?
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
GOLD ICE PAIN RELIEF
menthol creamProduct 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)