Label: POWER RELIEF- menthol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 64483-007-02 - Packager: Clientele, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 Label Information
Updated September 6, 2011
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Indications
- Warnings
- Directions
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 59.1 ml Bottle Label
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INGREDIENTS AND APPEARANCE
POWER RELIEF
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64483-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol 2 mL in 100 mL Inactive Ingredients Ingredient Name Strength Camphor (Synthetic) (UNII: 5TJD82A1ET) 0.52 mL in 100 mL Water (UNII: 059QF0KO0R) 84.61 mL in 100 mL Eucalyptus oil (UNII: 2R04ONI662) 0.81 mL in 100 mL Product Characteristics Color YELLOW Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64483-007-02 59 mL in 1 BOTTLE, WITH APPLICATOR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 04/02/2004 Labeler - Clientele, Inc. (085021806)
