Label: ETHYL ALCOHOL lotion
- NDC Code(s): 62832-447-69
- Packager: S.P. Richards Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 24, 2022
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- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- principal display panel
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INGREDIENTS AND APPEARANCE
ETHYL ALCOHOL
ethyl alcohol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62832-447 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol .62 mL in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) PEG-8 DIMETHICONE (UNII: GIA7T764OD) MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG) GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62832-447-69 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/03/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/03/2017 Labeler - S.P. Richards Company (007976384) Registrant - Vi-Jon, LLC (088520668) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(62832-447) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(62832-447)