Label: EUCALYPTAMINT- menthol ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 63736-340-02 - Packager: Insight Pharmaceuticals
- 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 July 20, 2009
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - Tube Label
- PRINCIPAL DISPLAY PANEL - Carton Label
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INGREDIENTS AND APPEARANCE
EUCALYPTAMINT
menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63736-340 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Menthol (UNII: L7T10EIP3A) (Menthol - UNII:L7T10EIP3A) Menthol 9.6 mL in 60 mL Inactive Ingredients Ingredient Name Strength Eucalyptus Oil (UNII: 2R04ONI662) Mineral Oil (UNII: T5L8T28FGP) Petrolatum (UNII: 4T6H12BN9U) Product Characteristics Color YELLOW Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63736-340-02 1 in 1 BOX 1 60 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/09/2009 Labeler - Insight Pharmaceuticals (176792315)