Label: AMOVEO ORIGINAL- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 49955-701-01, 49955-701-50 - Packager: Protair-X Health Solutions 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 February 24, 2017
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INGREDIENTS AND APPEARANCE
AMOVEO ORIGINAL
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49955-701 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 700 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49955-701-50 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/24/2017 2 NDC:49955-701-01 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/24/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/24/2017 Labeler - Protair-X Health Solutions Inc. (205614519)