Label: MIUS- ethyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71887-272-01 - Packager: MIUS Industries Corp
- 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 December 25, 2017
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- Active ingredient
- Purpose
- Uses
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- Directions
- Inactive ingredients
- MIUS hand sanitizer Label JPEG.jpeg
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INGREDIENTS AND APPEARANCE
MIUS
ethyl alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71887-272 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength ORANGE OIL, DISTILLED (UNII: H4QNH2ZN7A) GRAPEFRUIT OIL (UNII: YR377U58W9) SAFFLOWER OIL (UNII: 65UEH262IS) CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) APPLE CIDER VINEGAR (UNII: 0UE22Q87VC) TEA TREE OIL (UNII: VIF565UC2G) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Product Characteristics Color white (Transparent , foggy , might have traces of yellow from essential oils) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71887-272-01 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/17/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 01/17/2018 Labeler - MIUS Industries Corp (080937856)