Label: MIUS- ethyl alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71887-272-02 - 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 26, 2017
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warning
- Directions
- Inactive ingredients
- MIUS Natural Hand Sanitizer Free and Clear
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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 GLYCERIN (UNII: PDC6A3C0OX) APPLE CIDER VINEGAR (UNII: 0UE22Q87VC) SAFFLOWER OIL (UNII: 65UEH262IS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (Transparent, Foggy, may see separated oil) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71887-272-02 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) Registrant - MIUS Industries Corp. (080937856) Establishment Name Address ID/FEI Business Operations MIUS Industries Corp. 080937856 manufacture(71887-272) , label(71887-272)