Label: RASH RELIEF ANTIFUNGAL- miconazole liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 15071-804-11 - Packager: Touchless Care Concepts LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 November 16, 2011
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- Official Label (Printer Friendly)
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Active IngredientsMiconazole Nitrate 2% Dimethicone 10% Petrolatum 10%
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PurposeAntifungal / Skin Protectant
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Warnings- Ask a doctor before use on children under the age of two. For external use only. - When using this product do not get into eyes. - Stop use and ask a doctor if: irritation develops; there ...
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Directions- Clean the affected area and dry thoroughly. - Shake bottle well before use. - Spray 4-6 inches from skin twice daily (morning and night) or as directed by a physician. No rub-in is ...
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Inactive IngredientsCyclomethicone, Hexamethyldisiloxane, Lanolin, Light Mineral Oil, Microcrystalline Wax, Vitamin A Palmitate, Vitamin D3, Water, White Petrolatum
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INDICATIONS & USAGEUses: Treats jock itch, ringworm, and athlete's foot
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KEEP OUT OF REACH OF CHILDREN- Keep out of reach of children. If swallowed, get medical help or contact a local poison control center immediately
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information